List of diseases (C)

This is a list of diseases starting with the letter "C".

C

Ca

Cac–Cal


Cam–Can

Cap

  • Capillary leak syndrome with monoclonal gammopathy
  • Capillary venous leptomeningeal angiomatosis
  • Caplan's syndrome
  • Capos syndrome

Cara–Carc

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
  • Cardioskeletal myopathy-neutropenia
  • Cardiospasm

Care–Carr

Cart

Cas

  • Cassia–Stocco–Dos Santos syndrome
  • Castleman's disease
  • Castro–Gago–Pombo–Novo syndrome

Cat

Cata

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

Cera

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

Ch

Chag–Chao

Char

Charco

Charcot Charcot d

Charcot–Marie–Tooth disease

Charg–Charl

Chav

Che

Chi–Chl

Choa–Chol

Chon

Chor

Chri

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

  • 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

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

Cola–Coll

Colo–Colv

Com

Cond–Cone

Congen

Congenital a – Congenital b

Congenital c – Congenital g

Congenital h – Congenital l

Congenital m – Congenital s

Congenital t – Congenital v

Conges
Conju
  • Conjunctivitis ligneous
  • Conjunctivitis with pseudomembrane
  • Conjunctivitis

Conn–Conv

  • 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

Cor

Corm–Coro

Corp–Cort

Cos–Cox

Cr

Cram

Crand–Crane
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

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

Cy–Cz

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