MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
1,772 Erkrankungen gefunden (Malf.) Zurücksetzen

Cerebellar ataxia-ectodermal dysplasia syndrome

ORPHA:1174Malf.
Autosomal recessive

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

ORPHA:603448Malf.
Autosomal dominant

Cerebellar hypoplasia-tapetoretinal degeneration syndrome

ORPHA:2246Malf.

Cerebellar-facial-dental syndrome

ORPHA:444072Malf.
Autosomal recessive

Cerebrocostomandibular syndrome

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

Cerebrofacioarticular syndrome

ORPHA:314679Malf.
Autosomal recessive

Cerebrofaciothoracic dysplasia

ORPHA:1394Malf.
Autosomal recessive

Cerebrooculonasal syndrome

ORPHA:66625Malf.
Autosomal dominant

Char syndrome

ORPHA:46627Malf.
Autosomal dominant

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

ORPHA:90103Malf.
Autosomal recessive

Charlie M syndrome

ORPHA:1406Malf.
Not applicable

Cherubism

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

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

ORPHA:589856Malf.
Autosomal dominant

Chondrodysplasia punctata, Toriello type

ORPHA:79347Malf.
Autosomal recessive

Chondrodysplasia punctata, tibial-metacarpal type

ORPHA:79346Malf.
Unknown

Chondrodysplasia with joint dislocations, gPAPP type

ORPHA:280586Malf.
Autosomal recessive

Chondrodysplasia-difference of sex development syndrome

ORPHA:1422Malf.
Autosomal recessive

Choroidal atrophy-alopecia syndrome

ORPHA:1433Malf.
Unknown

Christianson syndrome

ORPHA:85278Malf.
X-linked recessive

Chromosome Y microdeletion syndrome

ORPHA:1646Malf.
Not applicable, Y-linked

Chudley-McCullough syndrome

ORPHA:314597Malf.
Autosomal recessive

Clark-Baraitser syndrome

ORPHA:600731Malf.

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

ORPHA:508476Malf.
Autosomal recessive

Cleft lip/palate-deafness-sacral lipoma syndrome

ORPHA:2003Malf.
Unknown