MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
1,772 diseases matched (Malform.) Reset

Cerebellar ataxia-ectodermal dysplasia syndrome

ORPHA:1174Malform.
Autosomal recessive

Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome

ORPHA:603448Malform.
Autosomal dominant

Cerebellar hypoplasia-tapetoretinal degeneration syndrome

ORPHA:2246Malform.

Cerebellar-facial-dental syndrome

ORPHA:444072Malform.
Autosomal recessive

Cerebrocostomandibular syndrome

ORPHA:1393Malform.
Autosomal dominant, Autosomal recessive, Not applicable

Cerebrofacioarticular syndrome

ORPHA:314679Malform.
Autosomal recessive

Cerebrofaciothoracic dysplasia

ORPHA:1394Malform.
Autosomal recessive

Cerebrooculonasal syndrome

ORPHA:66625Malform.
Autosomal dominant

Char syndrome

ORPHA:46627Malform.
Autosomal dominant

Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome

ORPHA:90103Malform.
Autosomal recessive

Charlie M syndrome

ORPHA:1406Malform.
Not applicable

Cherubism

ORPHA:184Malform.
Autosomal dominant, Autosomal recessive, Not applicable

Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome

ORPHA:589856Malform.
Autosomal dominant

Chondrodysplasia punctata, Toriello type

ORPHA:79347Malform.
Autosomal recessive

Chondrodysplasia punctata, tibial-metacarpal type

ORPHA:79346Malform.
Unknown

Chondrodysplasia with joint dislocations, gPAPP type

ORPHA:280586Malform.
Autosomal recessive

Chondrodysplasia-difference of sex development syndrome

ORPHA:1422Malform.
Autosomal recessive

Choroidal atrophy-alopecia syndrome

ORPHA:1433Malform.
Unknown

Christianson syndrome

ORPHA:85278Malform.
X-linked recessive

Chromosome Y microdeletion syndrome

ORPHA:1646Malform.
Not applicable, Y-linked

Chudley-McCullough syndrome

ORPHA:314597Malform.
Autosomal recessive

Clark-Baraitser syndrome

ORPHA:600731Malform.

Cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome

ORPHA:508476Malform.
Autosomal recessive

Cleft lip/palate-deafness-sacral lipoma syndrome

ORPHA:2003Malform.
Unknown