List of diseases (C)
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [1] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.
|
Diseases |
C
- C syndrome
- C1 esterase deficiency (angioedema)
Ca
Cac-Cal
- Cacchi-Ricci disease
- CACH syndrome
- Cacophobia
- Cafe au lait spots syndrome
- Caffey disease
- CAHMR syndrome
- Calcinosis cutis (see also CREST syndrome)
- Calciphylaxis
- Calculi
- Calderon Gonzalez Cantu syndrome
- Calloso genital dysplasia
- Callus disease
- Calpainopathy
- Calvarial hyperostosis
Cam-Can
- Camera Marugo -Cohen syndrome
- Camfak syndrome
- Campomelia Cumming type
- Camptobrachydactyly
- Camptocormism
- 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 leukodystrophy
- Cancer
- Candidiasis familial chronic
- Candidiasis
- 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
Cap
- Capillary leak syndrome with monoclonal gammopathy
- Capillary venous leptomeningeal angiomatosis
- Caplan's syndrome
- Capos syndrome
Car
Cara-Carc
- Caratolo Cilio Pessagno syndrome
- Carbamoyl phosphate synthetase deficiency
- Carbamoyl-phosphate synthase I deficiency disease (ornithine carbamoyl phosphate deficiency)
- Carbohydrate deficient glycoprotein syndrome
- Carbon baby syndrome
- Carbonic anhydrase II deficiency
- Carcinoid syndrome
- Carcinoma of the vocal tract
- Carcinoma, squamous cell of head and neck
- Carcinoma, squamous cell
- Carcinophobia
Card
Cardi
Cardia
- Cardiac amyloidosis
- Cardiac and laterality defects
- Cardiac arrest
- Cardiac conduction defect, familial
- Cardiac diverticulum
- Cardiac hydatid cysts with intracavitary expansion
- Cardiac malformation
- Cardiac tamponade
- Cardiac valvular dysplasia, X-linked
- pernambuco viadim
Cardio
- Cardioauditory syndrome of Sanchez- Cascos
- Cardioauditory syndrome
- Cardiofacial syndrome short limbs
- Cardiofaciocutaneous syndrome
- Cardiogenital syndrome
- Cardiomelic syndrome Stratton Koehler type
- Cardiomyopathy:
- Arrhythmogenic right ventricular cardiomyopathy
- Cardiomyopathic lentiginosis
- Cardiomyopathy cataract hip spine disease
- Cardiomyopathy diabetes deafness
- Dilated cardiomyopathy: Cardiomyopathy dilated with conduction defect type 1, Cardiomyopathy dilated with conduction defect type 2, Cardiomyopathy, familial dilated
- Cardiomyopathy due to anthracyclines
- Cardiomyopathy hearing loss type t RNA lysine gene mutation
- Hypertrophic cardiomyopathy: familial
- Cardiomyopathy hypogonadism metabolic anomalies
- Cardiomyopathy spherocytosis
- Cardiomyopathy, fatal fetal, due to myocardial calcification
- Cardiomyopathy, X linked, fatal infantile
- Restrictive cardiomyopathy
- Cardiophobia
- Cardioskeletal myopathy-neutropenia
- Cardiospasm
Care-Carr
- Carey Fineman Ziter syndrome
- Carnevale Canun Mendoza syndrome
- Carnevale Hernandez Castillo syndrome
- Carnevale Krajewska Fischetto syndrome
- Carney syndrome
- Carnitine palmitoyl transferase 1 deficiency
- Carnitine palmitoyl transferase 2 deficiency
- Carnitine palmitoyl transferase deficiency
- Carnitine transporter deficiency
- Carnitine-acylcarnitine translocase deficiency
- Carnophobia
- Carnosinase deficiency
- Carnosinemia
- Caroli disease
- Carotenemia
- Carotid artery dissection
- Carpal deformity migrognathia microstomia
- Carpal tunnel syndrome
- Carpenter Hunter type
- Carpenter syndrome
- Carpo tarsal osteolysis recessive
- Carpotarsal osteochondromatosis
- Carrington syndrome
Cart
- Cartilage-hair hypoplasia
- Cartilage hair hypoplasia like syndrome
- Cartilaginous neoplasms
- Cartwright Nelson Fryns syndrome
Cas
Cat
- Cat cry syndrome - see Cri du chat
- Cat Eye syndrome
- Cat Rodrigues syndrome
- Cat-scratch disease
Cata
- Catagelophobia
- Catapedaphobia
- Cataract,congenital ichthyosis
- 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-glaucoma
Catc-Cate
Cau-Cay
- Caudal appendage deafness
- Caudal duplication
- Caudal regression syndrome
- Causalgia
- Cavernous hemangioma
- Cavernous lymphangioma
- Cavernous sinus thrombosis
- Cayler syndrome
Cc-Cd
- CCA syndrome
- Ccge syndrome
- CCHS
- CDG syndrome type 1A
- CDG syndrome type 1B
- CDG syndrome type 1C
- CDG syndrome type 2
- CDG syndrome type 3
- CDG syndrome type 4
- CDG syndrome
- CDK4 linked melanoma
Ce
Cec-Cep
- Cecato De lima Pinheiro syndrome
- Celiac disease epilepsy occipital calcifications
- Celiac sprue
- Cenani Lenz syndactylism
- Cennamo Gangemi syndrome
- Central core disease
- Central diabetes insipidus
- Central nervous system protozoal infections
- Central serous chorioretinopathy
- Central type neurofibromatosis
- Centromeric instability immunodeficiency syndrome
- Centronuclear myopathy
- Centrotemporal epilepsy
- Cephalopolysyndactyly
Cer
Cera
Cere
Cereb
Cerebe
- Cerebellar agenesis
- Cerebellar ataxia areflexia pes cavus optic atrophy
- Cerebellar ataxia ectodermal dysplasia
- Cerebellar ataxia infantile with progressive external ophthalmoplegia
- Cerebellar ataxia, dominant pure
- Cerebellar degeneration, subacute
- Cerebellar degeneration
- Cerebellar hypoplasia endosteal sclerosis
- Cerebellar hypoplasia tapetoretinal degeneration
- Cerebellar hypoplasia
- Cerebellar parenchymal degeneration
- Cerebelloolivary atrophy
- Cerebelloparenchymal disorder 3
- Cerebellum agenesis hydrocephaly
Cerebr
- Cerebral Amyloid Angiopathy, Familial
- Cerebral amyloid angiopathy
- 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 jaw cysts
- Cerebral gigantism
- Cerebral hypoxia
- 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 genital syndrome
- Cerebro oculo skeleto renal syndrome
- Cerebro reno digital syndrome
- Cerebroarthrodigital syndrome
- Cerebro-costo-mandibular syndrome
- Cerebro-oculo-facio-skeletal syndrome
- Cerebroretinal vasculopathy
Cero-Cerv
- 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 lipofuscinois, neuronal
- Ceroid lipofuscinosis, neuronal 4
- Cervical cancer
- Cervical hypertrichosis neuropathy
- Cervical hypertrichosis peripheral neuropathy
- Cervical ribs sprengel anomaly polydactyly
- Cervical vertebral fusion
- Cervicooculoacoustic syndrome
Ch
Cha
Chag-Chao
- Chagas disease
- Chalazion
- Chanarin disease
- Chanarin Dorfman syndrome ichthyosis
- Chancroid
- Chandler's syndrome
- Chands syndrome
- Chang Davidson Carlson syndrome
- Chaotic atrial tachycardia
Char
Charc
Charco
Charcot Charcot d
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 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 disease
- Charcot-Marie-Tooth peroneal muscular atrophy, X-linked
Charg-Charl
Chav
Che
- Chediak-Higashi syndrome
- Cheilitis glandularis
- Chemke Oliver Mallek syndrome
- Chemodectoma
- Chemophobia
- Chen Kung Ho Kaufman Mcalister syndrome
- Cherubism
Chi-Chl
- Chiari type 1 malformation
- Chiari-Frommel syndrome
- Chickenpox
- Chikungunya
- CHILD syndrome ichthyosis
- Childhood disintegrative disorder
- Childhood pustular psoriasis
- Chimerism
- Chinese restaurant syndrome
- Chitayat Haj Chahine syndrome
- Chitayat Meunier Hodgkinson syndrome
- Chitayat Moore Del Bigio syndrome
- Chitty Hall Baraitser syndrome
- Chitty Hall Webb syndrome
- Chlamydia trachomatis
- Chlamydia
- Chlamydial and Gonococcal Conjunctivitis
Cho
Choa-Chol
- Choanal atresia deafness cardiac defects dysmorphia
- Cholangiocarcinoma
- Cholangitis, primary sclerosing
- Cholecystitis
- Choledochal cyst, hand malformation
- Cholelithiasis
- Cholemia, familial
- Cholera
- Cholerophobia
- Cholestasis pigmentary retinopathy cleft palate
- Cholestasis, progressive familial intrahepatic 1
- Cholestasis, progressive familial intrahepatic 2
- Cholestasis, progressive familial intrahepatic 3
- Cholestasis, progressive familial intrahepatic
- Cholestasis
- Cholestatic jaundice renal tubular insufficiency
- Cholesterol ester storage disease
- Cholesterol esterification disorder
- Cholesterol pneumonia
Chon
- Chondroblastoma
- Chondrocalcinosis familial articular
- Chondrocalcinosis
- Chondrodysplasia lethal recessive
- Chondrodysplasia pseudohermaphrodism syndrome
- Chondrodysplasia punctata 1, x-linked recessive
- Chondrodysplasia punctata with steroid sulfatase deficiency
- Chondrodysplasia punctata, brachytelephalangic
- Chondrodysplasia punctata, Sheffield type
- Chondrodysplasia punctata
- Chondrodysplasia situs inversus imperforate anus polydactyly
- Chondrodysplasia, Grebe type
- Chondrodystrophy
- Chondroectodermal dysplasia
- Chondroma (benign)
- Chondromalacia
- Chondromatosis (benign)
- Chondrosarcoma (malignant)
- Chondrysplasia punctata, humero-metacarpal type
Chor
- Chordoma
- Chorea acanthocytosis
- Chorea familial benign
- Chorea minor
- Chorea
- Choreoacanthocytosis amyotrophic
- Choreoathetosis familial paroxysmal
- Choriocarcinoma
- Chorioretinitis
- Chorioretinopathy dominant form microcephaly
- Choroid plexus cyst
- Choroid Plexus neoplasms
- Choroidal atrophy alopecia
- Choroideremia hypopituitarism
- Choroideremia
- Choroiditis, serpiginous
- Choroiditis
- Choroido cerebral calcification syndrome infantile
Chr
Chri
- Christian Demyer Franken syndrome
- Christian Johnson Angenieta syndrome
- Christian syndrome
- Christianson Fourie syndrome
- Christmas disease
Chro
Chrom
Chromo
Chromom-Chromop
Chromos Chromosoma
Chromosome Chromosome 1
- 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-Chromosome 12
- 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 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-Chromosome 15
- 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-Chromosome 1q
- Chromosome 16, trisomy 16p
- Chromosome 16, trisomy 16q
- Chromosome 16, trisomy
- Chromosome 16, uniparental disomy
- Chromosome 17 trisomy
- Chromosome 17 deletion
- Chromosome 17 ring
- 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 18p
- Chromosome 18, trisomy 18q
- Chromosome 18, trisomy
- Chromosome 19 ring
- Chromosome 19, trisomy 19q
- Chromosome 1q, duplication 1q12 q21
Chromosome 2
- 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-Chromosome 22
- 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 q11 q13
- Chromosome 22, trisomy
Chromosome 3
- 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-Chromosome 5
- 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-Chromosome 7
- 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 7q2
- Chromosome 7, monosomy 7q21
- Chromosome 7, monosomy 7q3
- Chromosome 7, monosomy
- 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-Chromosome 9
- 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 8p
- Chromosome 8, trisomy 8q
- Chromosome 8, trisomy
- 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 9q
- Chromosome 9, trisomy 9q32
- Chromosome 9, trisomy mosaic
- Chromosome 9, trisomy
Chromosomes
Chron
- Chronic berylliosis
- Chronic demyelinizing neuropathy with IgM monoclonal
- Chronic erosive gastritis
- Chronic fatigue immune dysfunction syndrome
- Chronic fatigue syndrome
- Chronic granulomatous disease
- Chronic hiccup
- Chronic inflammatory demyelinating polyneuropathy
- Chronic lymphocytic leukemia
- Chronic mountain sickness
- 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
Chu-Chy
- Chudley Lowry Hoar syndrome
- Chudley Rozdilsky syndrome
- Chudley-Mccullough syndrome
- Churg-Strauss syndrome
- Chylous ascites
Ci
- 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
- Cinchonism
- Circumscribed cutaneous aplasia of the vertex
- Circumscribed disseminated keratosis Jadassohn Lew type
- Citrullinemia
Cl
Cla
Cle
Clef
Cleft
Cleft h-Cleft l
- Cleft hand absent tibia
- 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 lip
- Cleft lower lip cleft lateral canthi chorioretinal
Cleft p-Cleft u
- 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 palate
- Cleft tongue syndrome
- Cleft upper lip median cutaneous polyps
Clefti
Clei
Cli-Clu
- Cloacal exstrophy
- Clouston syndrome
- Cloverleaf skull bone dysplasia
- Cloverleaf skull micromelia thoracic dysplasia
- Clubfoot
- Cluster headache
Cm
Co
Coa-Cof
- Coach syndrome
- Coal workers' pneumoconiosis
- Coarctation of aorta dominant
- Coarse face hypotonia constipation
- Coats disease
- Cocaine antenatal infection
- Cocaine fetopathy
- Coccidioidomycosis
- Cochin Jewish Disorder
- 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
Cog-Coh
- Cogan-Reese syndrome
- Cogan syndrome
- Cohen Hayden syndrome
- Cohen Lockood Wyborney syndrome
- Cohen syndrome
Col
Cola-Coll
- 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
- Collagen disorder
- Collagenous colitis
- Collins Pope syndrome
- Collins Sakati syndrome
Colo-Colv
- 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 type B brachydactyly
- Coloboma of macula
- 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 heart disease hearing
- Colobomatous microphthalmia
- Colon cancer, familial nonpolyposis
- Colonic atresia
- Colonic malakoplakia
- Color blindness
- Colorado tick fever
- Colver Steer Godman syndrome
Com
- 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
Con
Cond-Cone
- Conductive deafness malformed external ear
- Conductive hearing loss
- Condyloma acuminatum
- Condyloma
- Cone dystrophy
- Cone rod dystrophy amelogenesis imperfecta
- Cone rod dystrophy
Cong
Conge
Congen
Congenital a-Congenital b
- Congenital absence of the uterus and vagina
- 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 adrenal hyperplasia
- 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 c-Congenital g
- 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 gastrointestinal disorder
- Congenital generalized fibromatosis
- Congenital giant megaureter
Congenital h-Congenital l
- 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