MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Cardiomyopathy-cataract-hip spine disease syndrome

ORPHA:1345Kr.
Autosomal recessive

Cardiomyopathy-hypotonia-lactic acidosis syndrome

ORPHA:91130Kr.
Autosomal recessive

Caribbean parkinsonism

ORPHA:97355Kr.

Carney complex

ORPHA:1359Kr.
Autosomal dominant

Carney complex-trismus-pseudocamptodactyly syndrome

ORPHA:319340Kr.
Not applicable

Carney triad

ORPHA:139411Kr.

Carney-Stratakis syndrome

ORPHA:97286Kr.
Autosomal dominant

Carnitine palmitoyl transferase 1A deficiency

ORPHA:156Kr.
Autosomal recessive

Carnitine palmitoyltransferase II deficiency

ORPHA:157Kr.
Autosomal recessive

Carnitine-acylcarnitine translocase deficiency

ORPHA:159Kr.
Autosomal recessive

Carotid web

ORPHA:698260Kr.
Not applicable

Cartilage-hair hypoplasia

ORPHA:175Kr.
Autosomal recessive

Carvajal syndrome

ORPHA:65282Kr.
Autosomal dominant, Autosomal recessive

Castleman disease

ORPHA:160Kr.
Not applicable

Cat-scratch disease

ORPHA:50839Kr.
Not applicable

Cataract-ataxia-deafness syndrome

ORPHA:1368Kr.
Autosomal recessive

Cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome

ORPHA:436174Kr.
Autosomal recessive

Catastrophic antiphospholipid syndrome

ORPHA:464343Kr.
Not applicable

Catecholaminergic polymorphic ventricular tachycardia

ORPHA:3286Kr.
Autosomal dominant, Autosomal recessive

Cathepsin A-related arteriopathy-strokes-leukoencephalopathy

ORPHA:575553Kr.
Autosomal dominant

Cavitary myiasis

ORPHA:165958Kr.
Not applicable

Celiac artery compression syndrome

ORPHA:293208Kr.
Not applicable

Celiac disease-epilepsy-cerebral calcification syndrome

ORPHA:1459Kr.
Not applicable

Central areolar choroidal dystrophy

ORPHA:75377Kr.
Autosomal dominant