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List of diseases (C)



A list of diseases in the English wikipedia.

Diseases
Alphabetical list: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
See also: Health  |  Exercise  |  Nutrition



Contents

C

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

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

Cart

Cas

Cat

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

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

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

Char

  • Char syndrome
Charc
Charco

Charcot Charcot d

Charcot Marie Tooth disease

Charg-Charl

Chav

  • Chavany-Brunhes syndrome

Che

Chi-Chl

Cho

Choa-Chol

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

  • Chromosomal triplication

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

  • Chromosomes 1 and 2, monosomy 2q duplication 1p
Chron

Chu-Chy

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
  • Clefting ectropion conical teeth

Clei

Cli-Clu

Cm

Co

Coa-Cof

Cog-Coh

  • Cogan-Reese syndrome
  • Cogan syndrome
  • Cohen Hayden syndrome
  • Cohen Lockood Wyborney syndrome
  • Cohen syndrome

Col

Cola-Coll

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

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 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 m-Congenital s

  • 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
  • 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 t-Congenital v

  • Congenital toxoplasmosis
  • Congenital unilateral pulmonary hypoplasia
  • Congenital vagal hyperreflexivity
  • Congenital varicella syndrome
Conges
Conju
  • Conjunctivitis ligneous
  • Conjunctivitis with Pseudomembrane
  • Conjunctivitis

Conn-Conv

  • Connective tissue dysplasia Spellacy type
  • Connexin 26 anomaly
  • Conn's syndrome
  • Conotruncal heart malformations
  • Conradi-Hünermann 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 dominant form
  • Convulsions benign familial neonatal

Coo-Cop

  • Cooks syndrome
  • Cooley's anemia
  • Copper deficiency familial benign
  • Copper transport disease
  • Coprastasophobia
  • Coproporhyria

Cor

Corm-Coro

  • Cormier Rustin Munnich syndrome
  • Corneal anesthesia deafness mental retardation
  • Corneal cerebellar syndrome
  • Corneal crystals myopathy neuropathy
  • Corneal dystrophy
  • 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

Corp-Cort

  • Corpus callosum agenesis
  • Corpus callosum dysgenesis
  • 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

Cos-Cox

Cr

Cra

Cram

  • Cramer Niederdellmann syndrome
  • Cramp-fasciculations syndrome

Cran

Crand-Crane
  • Crandall syndrome
  • Crane-Heise syndrome
Crani
Cranio
  • Cranio osteoarthropathy

Cranioa-Craniom

  • 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 arthrogryposis progeroid appearance
  • Craniofacial dysostosis
  • Craniofacial dysynostosis
  • Craniofaciocardioskeletal syndrome
  • Craniofaciocervical osteoglyphic dysplasia
  • Craniofrontonasal dysplasia
  • Craniofrontonasal syndrome Teebi type
  • Craniometaphyseal dysplasia dominant type
  • Craniometaphyseal dysplasia recessive type
  • Craniomicromelic syndrome

Cranios-Craniot

  • Craniostenosis cataract
  • Craniostenosis with congenital heart disease mental retardation
  • Craniostenosis
  • 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, sagittal, with Dandy-Walker malformation and hydrocephalus
  • Craniosynostosis
  • Craniotelencephalic dysplasia

Craw

  • Crawfurd syndrome

Cre-Cro

Cry

  • Cryoglobulinemia
  • Cryophobia
  • Cryptococcosis
  • Cryptogenic organized pneumopathy
  • Cryptomicrotia brachydactyly syndrome excess fingers
  • Cryptomicrotia brachydactyly syndrome
  • Cryptophthalmos-syndactyly syndrome
  • Cryptorchidism arachnodactyly mental retardation
  • Cryroglobulinemia
  • Crystal deposit disease
  • Crystallophobia

Cu

Cul-Cus

  • 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

Cut

  • Cutaneous anthrax
  • Cutaneous larva migrans
  • Cutaneous lupus erythematosus
  • Cutaneous photosensitivity colitis lethal
  • Cutaneous T-cell lymphoma
  • Cutaneous vascularitis
  • Cutis Gyrata syndrome of Beare and Stevenson
  • Cutis gyratum acanthosis nigricans craniosynostosis
  • Cutis laxa, recessive
  • Cutis laxa corneal clouding mental retardation
  • Cutis laxa osteoporosis
  • Cutis laxa with joint laxity and retarded development
  • Cutis laxa, dominant type
  • Cutis laxa, recessive type 1
  • Cutis laxa, recessive type 2
  • Cutis laxa
  • Cutis marmorata telangiectatica congenita
  • Cutis verticis gyrata mental deficiency
  • Cutis verticis gyrata thyroid aplasia mental retardation
  • Cutis verticis gyrata
  • Cutler Bass Romshe syndrome

Cy-Cz

  • Cyclic neutropenia
  • Cyclic vomiting syndrome
  • Cyclosporosis
  • Cypress facial neuromusculoskeletal syndrome
  • Cystathionine beta synthetase deficiency
  • Cystic adenomatoid malformation of lung
  • Cystic angiomatosis of bone, diffuse
  • Cystic fibrosis gastritis megaloblastic anemia
  • Cystic fibrosis
  • Cystic hamartoma of lung and kidney
  • Cystic hygroma lethal cleft palate
  • Cystic hygroma
  • Cystic medial necrosis of aorta
  • Cystin transport, protein defect of
  • Cystinosis
  • Cystinuria
  • Cystinuria-lysinuria
  • Cytochrome C oxidase deficiency
  • Cytomegalic inclusion disease
  • Cytomegalovirus
  • Cytoplasmic body myopathy
  • Czeizel Losonci syndrome
  • Czeizel syndrome
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "List_of_diseases_(C)". A list of authors is available in Wikipedia.
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