C Syndrome
C1 esterase deficiency, (type 2 with ascites)
Cacchi Ricci disease
CACH syndrome
Cafe au lait spots syndrome
Caffey disease
CAHMR syndrome
Calcinosis cutis (see also CREST syndrome)
Calderon Gonzalez Cantu syndrome
Calloso genital dysplasia
Callus disease
Calvarial hyperostosis
Camera Marugo -Cohen syndrome
Camfak syndrome
Campomelic Syndrome
Camptodactyly fibrous tissue hyperplasia skeletal dysplasia
Camptodactyly joint contractures facial skeletal dysplasia
Camptodactyly overgrowth unusual facies
Camptodactyly syndrome Guadalajara type 1
Camptodactyly syndrome Guadalajara type 2
Camptodactyly taurinuria
Camptodactyly vertebral fusion
Camptomelic syndrome
Campylobacter infection
Camurati-Engelmann Disease
Canavan Disease
Canavan leukodystrophy
Cancer, Colon
Cancer, Prostate
Cancers, Skin, General
Candidiasis familial chronic
Canga's bead symptom
Canine distemper
Cantalamessa Baldini Ambrosi syndrome
Cantu Sanchez Corona Fragoso syndrome
Cantu Sanchez Corona Garcia syndrome
Cantu Sanchez Corona Hernandes syndrome
Capillary leak syndrome with monoclonal gammopathy
Capillary venous leptomeningeal angiomatosis
Capos syndrome
Caratolo Cilio Pessagno syndrome
Carbamoyl phosphate synthetase deficiency
Carbamyl Phosphate Synthetase Deficiency
Carbohydrate Deficient Glycoprotein Syndrome Type Ia
Carbon baby syndrome
Carbonic anhydrase II deficiency
Carboxylase Deficiency, Multiple
Carcinoid Syndrome
Carcinoma of the vocal tract
Carcinoma, Renal Cell
Carcinoma, Squamous Cell
Carcinoma, squamous cell of head and neck
Cardiac and laterality defects
Cardiac arrest
Cardiac conduction defect, familial
Cardiac diverticulum
Cardiac hydatid cysts with intracavitary expansion
Cardiac malformation
Cardiac valvular dysplasia, X-linked
Cardioauditory syndrome
Cardioauditory syndrome of Sanchez- Cascos
Cardiofacial syndrome short limbs
Cardiofaciocutaneous Syndrome
Cardiogenital syndrome
Cardiomelic syndrome Stratton Koehler type
Cardiomyopathic lentiginosis
Cardiomyopathy cataract hip spine disease
Cardiomyopathy diabetes deafness
Cardiomyopathy due to anthracyclines
Cardiomyopathy hearing loss type t RNA lysine gene mutation
Cardiomyopathy hypogonadism metabolic anomalies
Cardiomyopathy spherocytosis
Cardiomyopathy, fatal fetal, due to myocardial calcification
Cardiomyopathy, X linked, fatal infantile
Cardioskeletal myopathy-neutropenia
Carey Fineman Ziter syndrome
Carnevale Canun Mendoza syndrome
Carnevale Hernandez Castillo syndrome
Carnevale Krajewska Fischetto syndrome
Carney syndrome
Carnitine Deficiency Syndromes
Carnitine palmitoyl transferase 1 deficiency
Carnitine palmitoyl transferase 2 deficiency
Carnitine Palmitoyltransferase Deficiency
Carnitine transporter deficiency
Carnitine-acylcarnitine translocase deficiency
Carnosinase deficiency
Caroli Disease
Carpal deformity migrognathia microstomia
Carpal Tunnel Syndrome
Carpenter Hunter type
Carpenter Syndrome
Carpo tarsal osteolysis recessive
Carpotarsal osteochondromatosis
Carrington syndrome
Cartilage hair hypoplasia like syndrome
Cartilage-hair hypoplasia
Cartilaginous neoplasms
Cartwright Nelson Fryns syndrome
Cassia Stocco Dos Santos syndrome
Castleman's Disease
Castro Gago Pombo Novo syndrome
Cat cry syndrome - see Cri du chat
Cat Eye Syndrome
Cat Rodrigues syndrome
Cat Scratch Disease
Cataract aberrant oral frenula growth retardation
Cataract anterior polar dominant
Cataract ataxia deafness
Cataract cardiomyopathy
Cataract congenital autosomal dominant
Cataract congenital dominant non nuclear
Cataract congenital Volkmann type
Cataract congenital with microphthalmia
Cataract Dental Syndrome
Cataract Hutterite type
Cataract hypertrichosis mental retardation
Cataract mental retardation hypogonadism
Cataract microcornea syndrome
Cataract microphthalmia septal defect
Cataract skeletal anomalies
Cataract, alopecia, sclerodactyly
Cataract, congenital, with microcornea or slight microphthalmia
Cataract, total congenital
Cataract,congenital ichthyosis
CATCH 22 syndrome
Catecholamine hypertension
Catel Manzke Syndrome
Cat-scratch disease
Caudal appendage deafness
Caudal duplication
Caudal Regression Syndrome
Cavernous hemangioma
Cavernous lymphangioma
Cavernous Malformation
Cayler Syndrome
CCA syndrome
Ccge syndrome
CDG syndrome
CDG syndrome type 1A
CDG syndrome type 1B
CDG syndrome type 1C
CDG syndrome type 2
CDG syndrome type 3
CDG syndrome type 4
CDK4 linked melanoma
Cecato De lima Pinheiro syndrome
Celiac Disease
Celiac disease epilepsy occipital calcifications
Celiac sprue
Cenani Lenz syndactylism
Cennamo Gangemi syndrome
Central Core Disease
Central diabetes insipidus
Central Hypoventilation Syndrome, Congenital
Central nervous system protozoal infections
Central serous chorioretinopathy
Central type neurofibromatosis
Centromeric instability immunodeficiency syndrome
Centronuclear myopathy, congenital
Centrotemporal epilepsy
Ceramidase deficiency
Ceramide trihexosidosis
Cerebellar Agenesis
Cerebellar ataxia
Cerebellar ataxia areflexia pes cavus optic atrophy
Cerebellar ataxia ectodermal dysplasia
Cerebellar ataxia infantile with progressive external ophthalmoplegia
Cerebellar ataxia, dominant pure
Cerebellar degeneration
Cerebellar Degeneration, Subacute
Cerebellar hypoplasia
Cerebellar hypoplasia endosteal sclerosis
Cerebellar hypoplasia tapetoretinal degeneration
Cerebellar parenchymal degeneration
Cerebelloolivary atrophy
Cerebelloparenchymal disorder 3
Cerebellum agenesis hydrocephaly
Cerebral amyloid angiopathy
Cerebral Amyloid Angiopathy, Familial
Cerebral aneurysm
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Cerebral calcification cerebellar hypoplasia
Cerebral calcifications opalescent teeth phosphaturia
Cerebral cavernous malformation
Cerebral cavernous malformations
Cerebral gigantism
Cerebral gigantism jaw cysts
Cerebral malformations hypertrichosis claw hands
Cerebral Palsy
Cerebral thrombosis -
Cerebral ventricle neoplasm
Cerebro facio articular syndrome
Cerebro facio thoracic dysplasia
Cerebro oculo dento auriculo skeletal syndrome
Cerebro Oculo Facio Skeletal Syndrome
Cerebro oculo genital syndrome
Cerebro oculo skeleto renal syndrome
Cerebro reno digital syndrome
Cerebroarthrodigital syndrome
Cerebrocostomandibular Syndrome
Cerebro-oculo-facio-skeletal syndrome
Cerebroretinal vasculopathy
Ceroid lipofuscinois, neuronal
Ceroid lipofuscinois, neuronal 1, infantile
Ceroid lipofuscinois, neuronal 2, late infantile
Ceroid lipofuscinois, neuronal 3, juvenile
Ceroid lipofuscinois, neuronal 4, adult type
Ceroid lipofuscinois, neuronal 5, late infantile
Ceroid lipofuscinois, neuronal 6, late infantile
Ceroid lipofuscinosis, neuronal 4
Cervical cancer
Cervical hypertrichosis neuropathy
Cervical hypertrichosis peripheral neuropathy
Cervical ribs sprengel anomaly polydactyly
Cervical vertebral fusion
Cervicooculoacoustic syndrome
Chagas Disease
Chanarin disease
Chanarin Dorfman syndrome ichthyosis
Chandler's Syndrome
Chands syndrome
Chang Davidson Carlson syndrome
Chaotic atrial tachycardia
Char syndrome
Charcot disease
Charcot Marie Tooth Disease
Charcot Marie tooth disease deafness dominant type
Charcot Marie tooth disease deafness mental retardation
Charcot Marie Tooth disease deafness recessive type
Charcot Marie Tooth type 1 aplasia cutis congenita
Charcot-Marie-Tooth disease
Charcot-Marie-Tooth disease type 1A
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease type 1C
Charcot-Marie-Tooth disease type 2A
Charcot-Marie-Tooth disease type 2B1
Charcot-Marie-Tooth disease type 2B2
Charcot-Marie-Tooth disease type 2C
Charcot-Marie-Tooth disease type 2D
Charcot-Marie-Tooth disease type 4A
Charcot-Marie-Tooth disease type 4B
Charcot-Marie-Tooth disease with ptosis and parkinsonism
Charcot-Marie-Tooth disease, intermediate form
Charcot-Marie-Tooth disease, neuronal, type A
Charcot-Marie-Tooth disease, neuronal, type B
Charcot-Marie-Tooth disease, neuronal, type D
Charcot-Marie-Tooth disease, X-linked type 2, recessive
Charcot-Marie-Tooth disease, X-linked type 3, recessive
Charcot-Marie-Tooth peroneal muscular atrophy, X-linked
CHARGE Association
CHARGE Syndrome
Charles' Disease
Charlie M syndrome
Chavany-Brunhes syndrome
Chediak Higashi Syndrome
Cheilitis glandularis
Chemke Oliver Mallek syndrome
Chen Kung Ho Kaufman Mcalister syndrome
Chiari Frommel Syndrome
Chiari type 1 malformation
Chiari-Frommel syndrome
CHILD syndrome ichthyosis
Childhood disintegrative disorder
Childhood pustular psoriasis
Chitayat Haj Chahine syndrome
Chitayat Meunier Hodgkinson syndrome
Chitayat Moore Del Bigio syndrome
Chitty Hall Baraitser syndrome
Chitty Hall Webb syndrome
Chlamydia trachomatis
Chlamydial and Gonococcal Conjunctivitis
Choanal atresia deafness cardiac defects dysmorphia
Cholangitis, Primary Sclerosing
Choledochal cyst, hand malformation
Cholemia, familial
Cholestasis pigmentary retinopathy cleft palate
Cholestasis, progressive familial intrahepatic
Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 2
Cholestasis, progressive familial intrahepatic 3
Cholestatic jaundice renal tubular insufficiency
Cholesterol ester storage disease
Cholesterol esterification disorder
Cholesterol pneumonia
Chondroblastoma (benign)
Chondrocalcinosis, Familial Articular
Chondrodysplasia lethal recessive
Chondrodysplasia pseudohermaphrodism syndrome
Chondrodysplasia punctata
Chondrodysplasia punctata 1, x-linked recessive
Chondrodysplasia punctata with steroid sulfatase deficiency
Chondrodysplasia punctata, brachytelephalangic
Chondrodysplasia punctata, Sheffield type
Chondrodysplasia situs inversus imperforate anus polydactyly
Chondrodysplasia, Grebe type
Chondroectodermal dysplasia
Chondroma (benign)
Chondromatosis (benign)
Chondrosarcoma (malignant)
Chondrysplasia punctata, humero-metacarpal type
Chorea acanthocytosis
Chorea familial benign
Chorea minor
Chorea, Sydenham's
Choreoacanthocytosis amyotrophic
Choreoathetosis familial paroxysmal
Chorioretinopathy dominant form microcephaly
Choroid plexus cyst
Choroid Plexus neoplasms
Choroidal atrophy alopecia
Choroideremia hypopituitarism
Choroiditis, Serpiginous
Choroido cerebral calcification syndrome infantile
Christian Demyer Franken syndrome
Christian Johnson Angenieta syndrome
Christian syndrome
Christianson Fourie syndrome
Christmas disease
Chromophobe renal carcinoma
Chromosomal triplication
Chromosome 1 ring
Chromosome 1, 1p36 deletion syndrome
Chromosome 1, deletion q21 q25
Chromosome 1, duplication 1p21 p32
Chromosome 1, monosomy 1p
Chromosome 1, monosomy 1p22 p13
Chromosome 1, monosomy 1p31 p22
Chromosome 1, monosomy 1p32
Chromosome 1, monosomy 1p34 p32
Chromosome 1, monosomy 1q25 q32
Chromosome 1, monosomy 1q32 q42
Chromosome 1, monosomy 1q4
Chromosome 1, q42 11 q42 12 duplication
Chromosome 1, trisomy 1q32 qter
Chromosome 1, trisomy 1q42 qter
Chromosome 1, uniparental disomy 1q12 q21
Chromosome 10 ring
Chromosome 10, Distal Trisomy 10q
Chromosome 10, Monosomy 10p
Chromosome 10, monosomy 10q
Chromosome 10, trisomy 10p
Chromosome 10, trisomy 10pter p13
Chromosome 10, trisomy 10q
Chromosome 10, uniparental disomy of
Chromosome 10p terminal deletion syndrome
Chromosome 11, deletion 11p
Chromosome 11, Partial Monosomy 11q
Chromosome 11, Partial Trisomy 11q
Chromosome 11-14 translocation
Chromosome 11p, partial deletion
Chromosome 11q partial deletion
Chromosome 11q trisomy
Chromosome 12 ring
Chromosome 12, 12p trisomy
Chromosome 12, trisomy 12q
Chromosome 12p deletion
Chromosome 12p partial deletion
Chromosome 13 duplication
Chromosome 13 ring
Chromosome 13, Partial Monosomy 13q
Chromosome 13p duplication
Chromosome 13q deletion
Chromosome 13q trisomy
Chromosome 13q-mosaicism
Chromosome 14 Ring
Chromosome 14 trisomy
Chromosome 14, deletion 14q, partial duplication 14p
Chromosome 14, Trisomy Mosaic
Chromosome 14q, partial deletions
Chromosome 14q, proximal duplication
Chromosome 14q, terminal deletion
Chromosome 14q, terminal duplication
Chromosome 15 Ring
Chromosome 15, Distal Trisomy 15q
Chromosome 15, trisomy mosaicism
Chromosome 15q, partial deletion
Chromosome 15q, tetrasomy
Chromosome 15q, trisomy
Chromosome 16, trisomy
Chromosome 16, trisomy 16p
Chromosome 16, trisomy 16q
Chromosome 16, uniparental disomy
Chromosome 17 deletion
Chromosome 17 ring
Chromosome 17 trisomy
Chromosome 17, deletion 17q23 q24
Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p11 2
Chromosome 17, trisomy 17q22
Chromosome 18 long arm deletion syndrome
Chromosome 18 mosaic monosomy
Chromosome 18 Ring
Chromosome 18, deletion 18q23
Chromosome 18, Monosomy 18p
Chromosome 18, Tetrasomy 18p
Chromosome 18, trisomy
Chromosome 18, trisomy 18p
Chromosome 18q- Syndrome
Chromosome 19 ring
Chromosome 19, trisomy 19q
Chromosome 1q, duplication 1q12 q21
Chromosome 2, monosomy 2p22
Chromosome 2, monosomy 2pter p24
Chromosome 2, monosomy 2q
Chromosome 2, monosomy 2q24
Chromosome 2, monosomy 2q37
Chromosome 2, trisomy 2p
Chromosome 2, Trisomy 2p13 p21
Chromosome 2, trisomy 2pter p24
Chromosome 2, trisomy 2q
Chromosome 2, trisomy 2q37
Chromosome 20 ring
Chromosome 20, deletion 20p
Chromosome 20, duplication 20p
Chromosome 20, trisomy
Chromosome 21 monosomy
Chromosome 21 Ring
Chromosome 21, monosomy 21q22
Chromosome 21, tetrasomy 21q
Chromosome 21, uniparental disomy of
Chromosome 22 Ring
Chromosome 22 trisomy mosaic
Chromosome 22, microdeletion 22 q11
Chromosome 22, monosome mosaic
Chromosome 22, Trisomy Mosaic
Chromosome 22, trisomy q11 q13
Chromosome 3 duplication syndrome
Chromosome 3, monosomy 3p
Chromosome 3, monosomy 3p14 p11
Chromosome 3, Monosomy 3p2
Chromosome 3, monosomy 3p25
Chromosome 3, monosomy 3q13
Chromosome 3, monosomy 3q21 23
Chromosome 3, monosomy 3q27
Chromosome 3, trisomy 3p
Chromosome 3, trisomy 3p25
Chromosome 3, trisomy 3q
Chromosome 3, trisomy 3q13 2 q25
Chromosome 3, Trisomy 3q2
Chromosome 4 Ring
Chromosome 4 short arm deletion
Chromosome 4, monosomy 4p14 p16
Chromosome 4, Monosomy 4q
Chromosome 4, monosomy 4q32
Chromosome 4, Monosomy Distal 4q
Chromosome 4, Partial Trisomy Distal 4q
Chromosome 4, Trisomy 4p
Chromosome 4, trisomy 4q
Chromosome 4, trisomy 4q21
Chromosome 4, trisomy 4q25 qter
Chromosome 5, monosomy 5q35
Chromosome 5, Trisomy 5p
Chromosome 5, trisomy 5pter p13 3
Chromosome 5, trisomy 5q
Chromosome 5, uniparental disomy
Chromosome 6 Ring
Chromosome 6, deletion 6q13 q15
Chromosome 6, monosomy 6p23
Chromosome 6, monosomy 6q
Chromosome 6, monosomy 6q1
Chromosome 6, monosomy 6q2
Chromosome 6, Partial Trisomy 6q
Chromosome 6, trisomy 6p
Chromosome 6, trisomy 6q
Chromosome 7 ring
Chromosome 7, monosomy
Chromosome 7, monosomy 7q2
Chromosome 7, monosomy 7q21
Chromosome 7, monosomy 7q3
Chromosome 7, Partial Monosomy 7p
Chromosome 7, trisomy 7p
Chromosome 7, trisomy 7p13 p12 2
Chromosome 7, trisomy 7q
Chromosome 7, trisomy mosaic
Chromosome 8 deletion
Chromosome 8 ring
Chromosome 8, monosomy 8p
Chromosome 8, Monosomy 8p2
Chromosome 8, monosomy 8p23 1
Chromosome 8, monosomy 8q
Chromosome 8, mosaic trisomy
Chromosome 8, partial trisomy
Chromosome 8, trisomy
Chromosome 8, trisomy 8p
Chromosome 8, trisomy 8q
Chromosome 9 inversion or duplication
Chromosome 9 Ring
Chromosome 9, duplication 9q21
Chromosome 9, monosomy 9p
Chromosome 9, Partial Monosomy 9p
Chromosome 9, partial trisomy 9p
Chromosome 9, Tetrasomy 9p
Chromosome 9, trisomy
Chromosome 9, Trisomy 9p (Multiple Variants)
Chromosome 9, trisomy 9q
Chromosome 9, trisomy 9q32
Chromosome 9, Trisomy Mosaic
Chromosomes 1 and 2, monosomy 2q duplication 1p
Chronic berylliosis
Chronic demyelinizing neuropathy with IgM monoclonal
Chronic erosive gastritis
Chronic fatigue immune dysfunction syndrome
Chronic Fatigue Syndrome
Chronic Fatigue Syndrome/Myalgic Encephalomyelitis
Chronic granulomatous disease
Chronic hiccup
Chronic Inflammatory Demyelinating Polyneuropathy
Chronic lymphocytic leukemia
Chronic myelogenous leukemia
Chronic myelomonocytic leukemia
Chronic necrotizing vasculitis
Chronic neutropenia
Chronic obstructive pulmonary disease
Chronic polyradiculoneuritis
Chronic recurrent multifocal osteomyelitis
Chronic renal failure
Chronic spasmodic dysphonia
Chronic, infantile, neurological, cutaneous, articular syndrome
Chudley Lowry Hoar syndrome
Chudley Rozdilsky syndrome
Chudley-Mccullough syndrome
Churg Strauss Syndrome
Chylous ascites
Cicatricial pemphigoid
Ciguatera Fish Poisoning
Ciliary discoordination, due to random ciliary orientation
Ciliary dyskinesia, due to transposition of ciliary microtubules
Ciliary dyskinesia-bronchiectasis
Cilliers Beighton syndrome
Circumscribed cutaneous aplasia of the vertex
Circumscribed disseminated keratosis Jadassohn Lew type
Cirrhosis, Primary Biliary
Clarkson disease
Clayton Smith Donnai syndrome
Cleft hand absent tibia
Cleft lip
Cleft lip and palate malrotation cardiopathy
Cleft lip and/or palate with mucous cysts of lower
Cleft lip palate abnormal thumbs microcephaly
Cleft lip palate deafness sacral lipoma
Cleft lip palate dysmorphism Kumar type
Cleft lip palate ectrodactyly
Cleft lip palate incisor and finger anomalies
Cleft lip palate mental retardation corneal opacity
Cleft lip palate oligodontia syndactyly pili torti
Cleft lip palate pituitary deficiency
Cleft lip palate-tetraphocomelia
Cleft lip with or without cleft palate
Cleft lower lip cleft lateral canthi chorioretinal
Cleft palate
Cleft Palate and Cleft Lip
Cleft palate cardiac defect ectrodactyly
Cleft palate colobomata radial synostosis deafness
Cleft palate heart disease polydactyly absent tibia
Cleft palate lateral synechia syndrome
Cleft palate short stature vertebral anomalies
Cleft palate stapes fixation oligodontia
Cleft palate X linked
Cleft tongue syndrome
Cleft upper lip median cutaneous polyps
Clefting ectropion conical teeth
Cleidocranial Dysplasia
Cleidocranial dysplasia micrognathia absent thumbs
Cloacal exstrophy
Clouston syndrome
Cloverleaf skull bone dysplasia
Cloverleaf skull micromelia thoracic dysplasia
Cluster headache
CMV antenatal infection
Coach syndrome
Coal worker's pneumoconiosis
Coarctation of aorta dominant
Coarse face hypotonia constipation
Coats' Disease
Cocaine antenatal infection
Cocaine fetopathy
Cochin Jewish Disorder
Cockayne Syndrome
Cockayne syndrome type 1
Cockayne syndrome type 2
Cockayne syndrome type 3
Cockayne's syndrome
Codas syndrome
Coenzyme Q cytochrome c reductase deficiency of
Coffin Lowry Syndrome
Coffin Siris Syndrome
COFS syndrome
Cogan Reese Syndrome
Cogan's syndrome
Cohen Hayden syndrome
Cohen Lockood Wyborney syndrome
Cohen Syndrome
Colavita Kozlowski syndrome
Cold agglutination syndrome
Cold agglutinin disease
Cold antibody hemolytic anemia
Cold contact urticaria
Cold urticaria
Cole carpenter syndrome
Coleman Randall syndrome
Colitis, Collagenous
Colitis, Ulcerative
Collagen disorder
Collagenous colitis
Collins Pope syndrome
Collins Sakati syndrome
Coloboma chorioretinal cerebellar vermis aplasia
Coloboma hair abnormality
Coloboma of choroid and retina
Coloboma of eye lens
Coloboma of iris
Coloboma of lens ala nasi
Coloboma of macula
Coloboma of macula type B brachydactyly
Coloboma of optic nerve
Coloboma of optic papilla
Coloboma porencephaly hydronephrosis
Coloboma uveal with cleft lip palate and mental retardation
Coloboma, ocular
Colobomata unilobar lung heart defect
Colobomatous microphthalmia
Colobomatous microphthalmia heart disease hearing
Colon cancer, familial nonpolyposis
Colonic atresia
Colonic malakoplakia
Color blindness
Colorado Tick Fever
Colver Steer Godman syndrome
Combarros Calleja Leno syndrome
Combined hyperlipidemia, familial
Common cold
Common mesentery
Common Variable Immunodeficiency
Compartment syndrome
Complement component 2 deficiency
Complement component receptor 1
Complete atrioventricular canal
Complex 1 mitochondrial respiratory chain deficiency
Complex 2 mitochondrial respiratory chain deficiency
Complex 3 mitochondrial respiratory chain deficiency
Complex 4 mitochondrial respiratory chain deficiency
Complex 5 mitochondrial respiratory chain deficiency
Complex regional pain syndrome
Conductive deafness malformed external ear
Conductive hearing loss
Condyloma acuminatum
Cone Dystrophy
Cone rod dystrophy
Cone rod dystrophy amelogenesis imperfecta
Congenital absence of the uterus and vagina
Congenital adrenal hyperplasia
Congenital adrenal hyperplasia type 1
Congenital adrenal hyperplasia type 2
Congenital adrenal hyperplasia type 3
Congenital adrenal hyperplasia type 4
Congenital adrenal hyperplasia type 5
Congenital afibrinogenemia
Congenital alopecia X linked
Congenital amputation
Congenital aneurysms of the great vessels
Congenital antithrombin III deficiency
Congenital aplastic anemia
Congenital arteriovenous shunt
Congenital articular rigidity
Congenital benign spinal muscular atrophy dominant
Congenital brain disorder
Congenital bronchobiliary fistula
Congenital cardiovascular disorder
Congenital cardiovascular malformations
Congenital cardiovascular shunt
Congenital constricting band
Congenital contractual arachnodactyly
Congenital contractures
Congenital craniosynostosis maternal hyperthyroiditis
Congenital cystic adenomatoid malformation
Congenital cystic eye multiple ocular and intracranial anomalies
Congenital cytomegalovirus
Congenital deafness
Congenital diaphragmatic hernia
Congenital erythropoietic porphyria
Congenital facial diplegia
Congenital fiber type disproportion
Congenital Fibrosis of the Extraocular Muscles
Congenital gastrointestinal disorder
Congenital generalized fibromatosis
Congenital giant megaureter
Congenital heart block
Congenital heart disease ptosis hypodontia craniostosis
Congenital heart disease radio ulnar synostosis mental retardation
Congenital heart disorder
Congenital heart septum defect
Congenital hemidysplasia with ichtyosiform erythroderma and limbs defects
Congenital hemolytic anemia
Congenital hepatic fibrosis
Congenital hepatic porphyria
Congenital herpes simplex
Congenital hypomyelination neuropathy
Congenital hypothyroidism
Congenital hypotrichosis milia
Congenital ichthyosis
Congenital ichthyosis, microcephalus, quadriplegia
Congenital ichtyosiform erythroderma
Congenital kidney disorder
Congenital lobar emphysema
Congenital megacolon
Congenital megalo-ureter
Congenital mesoblastic nephroma
Congenital microvillous atrophy
Congenital mitral malformation
Congenital mitral stenosis
Congenital mixovirus
Congenital mumps
Congenital muscular dystrophy syringomyelia
Congenital myopathy
Congenital nephrotic syndrome, Finnish type
Congenital nonhemolytic jaundice
Congenital rubella
Congenital short bowel
Congenital short femur
Congenital skeletal disorder
Congenital skin disorder
Congenital spherocytic anemia
Congenital spherocytic hemolytic anemia
Congenital stenosis of cervical medullary canal
Congenital sucrose isomaltose malabsorption
Congenital syphilis
Congenital toxoplasmosis
Congenital unilateral pulmonary hypoplasia
Congenital vagal hyperreflexivity
Congenital Varicella Syndrome
Congestive heart disease
Conjunctivitis with Pseudomembrane
Conjunctivitis, Ligneous
Conn Syndrome
Connective tissue dysplasia Spellacy type
Connexin 26 anomaly
Conotruncal heart malformations
Conradi Hunermann Syndrome
Constitutional growth delay
Constrictive bronchiolitis
Continuous muscle fiber activity hereditary
Continuous spike-wave during slow sleep syndrome
Contractural arachnodactyly
Contractures ectodermal dysplasia cleft lip palate
Contractures hyperkeratosis lethal
Contractures of feet-muscle atrophy-oculomotor apraxia
Conversion Disorder
Convulsions benign familial neonatal
Convulsions benign familial neonatal dominant form
Cooks syndrome
Cooley's anemia
Copper deficiency familial benign
Copper transport disease
Cor biloculare
Cor pulmonale
Cor Triatriatum
Cormier Rustin Munnich syndrome
Corneal anesthesia deafness mental retardation
Corneal cerebellar syndrome
Corneal crystals myopathy neuropathy
Corneal Dystrophies
Corneal dystrophy epithelial short stature
Corneal dystrophy ichthyosis microcephaly mental retardation
Corneal dystrophy perceptive deafness
Corneal dystrophy pigmentary anomaly malabsorption
Corneal endothelium dystrophy
Cornelia de Lange Syndrome
Corneodermatoosseous syndrome
Coronal synostosis syndactyly jejunal atresia
Coronaro-cardiac fistula
Coronary arteries congenital malformation
Coronary artery aneurysm
Coronary heart disease
Corpus callosum agenesis
Corpus callosum agenesis double urinary collecting
Corpus callosum agenesis neuronopathy
Corpus callosum agenesis of blepharophimosis Robin type
Corpus callosum agenesis of with chorioretinal abnormalities
Corpus callosum agenesis polysyndactyly
Corpus callosum dysgenesis cleft spasm
Corpus callosum dysgenesis hypopituitarism
Corpus callosum dysgenesis X linked recessive
Corsello Opitz syndrome
Cortada Koussef Matsumoto syndrome
Cortes Lacassie syndrome
Cortical blindness mental retardation polydactyly
Cortical degeneration of the cerebellum parenchymatous
Cortical dysplasia
Cortical hyperostosis syndactyly
Corticobasal Degeneration
Costello Syndrome
Costochondritis (otherwise Costal chondritis)
Costocoracoid ligament congenitally short
Cote Adamopoulos Pantelakis syndrome
Cote Katsantoni syndrome
Cousin Walbraum Cegarra syndrome
Covesdem syndrome
Cowchock Wapner Kurtz syndrome
Cowden's disease
Coxoauricular syndrome
Cramer Niederdellmann syndrome
Cramp-fasciculations syndrome
Crandall syndrome
Crane-Heise syndrome
Cranio osteoarthropathy
Cranioacrofacial syndrome
Craniodiaphyseal dysplasia
Craniodigital syndrome mental retardation
Cranioectodermal dysplasia
Craniofacial and osseous defects mental retardation
Craniofacial and skeletal defects
Craniofacial deafness hand syndrome
Craniofacial dysostosis
Craniofacial dysostosis arthrogryposis progeroid appearance
Craniofacial dysynostosis
Craniofaciocardioskeletal syndrome
Craniofaciocervical osteoglyphic dysplasia
Craniofrontonasal Dysplasia
Craniofrontonasal syndrome Teebi type
Craniometaphyseal Dysplasia
Craniometaphyseal dysplasia dominant type
Craniometaphyseal dysplasia recessive type
Craniomicromelic syndrome
Craniostenosis cataract
Craniostenosis with congenital heart disease mental retardation
Craniosynostosis alopecia brain defect
Craniosynostosis arthrogryposis cleft palate
Craniosynostosis autosomal dominant
Craniosynostosis cleft lip palate arthrogryposis
Craniosynostosis contractures cleft
Craniosynostosis exostoses nevus epibulbar dermoid
Craniosynostosis fibular aplasia
Craniosynostosis Fontaine type
Craniosynostosis Maroteaux Fonfria type
Craniosynostosis mental retardation clefting syndrome
Craniosynostosis mental retardation heart defects
Craniosynostosis Philadelphia type
Craniosynostosis radial aplasia syndrome
Craniosynostosis synostoses hypertensive nephropathy
Craniosynostosis Warman type
Craniosynostosis, Primary
Craniosynostosis, sagittal, with Dandy-Walker malformation and hydrocephalus
Craniotelencephalic dysplasia
Crawfurd syndrome
Creatine deficiency
Creeping disease
CREST syndrome (Calcinosis Raynaud's Esophagus Sclerodactyly Telangiectasia)
Cretinism athyreotic
Creutzfeldt Jakob Disease
Cri du Chat Syndrome
Crigler Najjar Syndrome Type I
Crisponi syndrome
Criss cross syndrome
Criswick-Schepens syndrome
Crohn's Disease
Crohn's disease of the esophagus
Crome syndrome
Cronkhite-Canada Syndrome
Crossed polydactyly type 1
Crossed polysyndactyly
Crouzon Syndrome
Crouzonodermoskeletal syndrome
Crow-Fukase syndrome
Cryoglobulinemia, Essential Mixed
Cryptogenic organized pneumopathy
Cryptomicrotia brachydactyly syndrome
Cryptomicrotia brachydactyly syndrome excess fingers
Cryptophthalmos-syndactyly syndrome
Cryptorchidism arachnodactyly mental retardation
Crystal deposit disease
Culler Jones syndrome
Curly hair ankyloblepharon nail dysplasia syndrome
Currarino triad
Curry Hall syndrome
Curth-Macklin type ichthyosis hystrix
Curtis Rogers Stevenson syndrome
Cushing syndrome, familial
Cushing's symphalangism
Cushing's Syndrome
Cutaneous anthrax
Cutaneous larva migrans
Cutaneous lupus erythematosus
Cutaneous photosensitivity colitis lethal
Cutaneous T-Cell Lymphomas
Cutaneous vascularitis
Cutis Gyrata syndrome of Beare and Stevenson
Cutis gyratum acanthosis nigricans craniosynostosis
Cutis Laxa
Cutis laxa corneal clouding mental retardation
Cutis laxa osteoporosis
Cutis laxa with joint laxity and retarded development
Cutis laxa, dominant type
Cutis laxa, recessive
Cutis laxa, recessive type 1
Cutis laxa, recessive type 2
Cutis Marmorata Telangiectatica Congenita
Cutis verticis gyrata
Cutis verticis gyrata mental deficiency
Cutis verticis gyrata thyroid aplasia mental retardation
Cutler Bass Romshe syndrome
Cyclic neutropenia
Cyclic Vomiting Syndrome
Cypress facial neuromusculoskeletal syndrome
Cystathionine beta synthetase deficiency
Cystic adenomatoid malformation of lung
Cystic angiomatosis of bone, diffuse
Cystic Fibrosis
Cystic fibrosis gastritis megaloblastic anemia
Cystic hamartoma of lung and kidney
Cystic Hygroma
Cystic hygroma lethal cleft palate
Cystic medial necrosis of aorta
Cystin transport, protein defect of
Cytochrome C Oxidase Deficiency
Cytomegalic inclusion disease
Cytomegalovirus Infection
Cytoplasmic body myopathy
Czeizel Losonci syndrome
Czeizel syndrome




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**Obese people less likely to survive colorectal cancer

According to a new report, people who are physically inactive and are obese around the middle have poor odds of survival after a diagnosis of colorectal cancer.

"We have now shown that modifiable lifestyle factors that were known to reduce the incidence of colorectal cancer can also reduce the mortality in cases diagnosed with the disease," Dr. Andrew M. M. Haydon told Reuters Health. "This strengthens the argument supporting the public health message of 'healthy living.'"

Haydon, from Monash Medical School in Melbourne, Australia, studied records from more than 40,000 patients diagnosed with colorectal cancer between 1990 and 1994.

Patients who got regular exercise before their colorectal cancer was found were 31 percent less likely to die from the cancer than were non-exercisers, the investigators report in the medical journal Gut. In fact, 73 percent of exercisers survived at least five years, compared with 61 percent of non-exercisers.

Such an improvement in survival "is at least as large as" as is usually achieved by add-on chemotherapy.

A greater percentage of body fat, bigger waist circumference, and/or greater weight were also associated with worse survival, according to the report.

**Study shows short term sex life improvements in prostate cancer survivors

It is well known that many men who undergo prostate cancer treatment (surgery or radiation therapy) have sexual dysfunction. A recent study of 84 prostate cancer survivors attempted to determine the impact of post-treatment interventions such as counseling sessions.

The study found that a large percentage of those who completed four therapy sessions reported better sexual functioning 3 months later. Counseling sessions focused on better communication between partners, ED treatment options, and methods of enjoying sex in spite of ED.

Both partners reported improvements in their sex life for up to 3 months later. There was also an increase in the number of men using ED treatments such as Viagra.

However, after six months the improvements began to wane. The researchers speculated that couples tended to revert back to old habits, and there also might have been greater reliance put on the "magic pill" solution. Drugs such as Viagra tend to have a lower success rate in prostate cancer survivors, so when these drugs stop working couples may adopt a defeatist attitude.

**Vitamin D helps fight cancer, report claims

A research team from the San Diego Moores Cancer Center headed up by Dr. Cedric Garland recently concluded that Vitamin D deficiency is often associated with various types of cancer. Dr. Garland now advises people to increase their intake of Vitamin D through diet or a vitamin supplement.

The research team reviewed 63 studies conducted between 1966 and 2004 on the relationship between vitamin D and certain types of cancer. The report concluded that Vitamin D deficiency was a factor in several thousand deaths due to colon, breast, ovarian and other cancers every year.

The report recommended increasing Vitamin D intake, either in the form of supplements or by eating certain foods such as fortified orange juice, yogurt and cheeses. This is especially the case with people in northern latitudes where there is less exposure to the sun. African Americans are also more prone to a Vitamin D deficiency because the their skin pigment reduces the amount produced by the body.

Observers welcomed the University of California study but also warned that kidney and liver damage could result from too much vitamin D.

The "natural" form of the vitamin, called D3, is normally produced in the skin after exposure to sunlight, but is also obtained from certain foods such as oily fish, margarine and meat.

**Resveratrol found in grapes helps fix our aching joints

Researchers at the American College of Rheumatology in San Diego, California have found that resveratrol found in red wine appears to halt cartilage damage caused by osteoarthritis, and speed up recovery.

It is thought that oxygen-rich particles in the blood cause severe damage to body cells similar to the way rust rots a car. Resveratrol is a powerful anti-oxidant which seems to function as a way to prevent this kind of injury.

The research found that resveratrol resulted in a reduction of between 50 and 90% of the production of chemicals that cause inflammation in the joints. It also enhanced production of specific proteins that are part of the connective tissue in joints.

Red wine has other beneficial effects on the body. It contains polyphenrols that reduce the amount of bad LDL cholesterol in the arteries. It also increases the amount of good HDL cholesterol.

Tannin and resveratrol, the anti-oxydants found in red wine, help to guard against cancer and slow tumor growth.

About The Author:
Rick Hendershot publishes Linknet News ==> | For information on name brand prescription drugs, visit | To fight childhood obesity see

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