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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 3,968 заболеваний (Disease) Сброс

Cardiomyopathy-cataract-hip spine disease syndrome

ORPHA:1345Disease
Autosomal recessive

Cardiomyopathy-hypotonia-lactic acidosis syndrome

ORPHA:91130Disease
Autosomal recessive

Caribbean parkinsonism

ORPHA:97355Disease

Carney complex

ORPHA:1359Disease
Autosomal dominant

Carney complex-trismus-pseudocamptodactyly syndrome

ORPHA:319340Disease
Not applicable

Carney triad

ORPHA:139411Disease

Carney-Stratakis syndrome

ORPHA:97286Disease
Autosomal dominant

Carnitine palmitoyl transferase 1A deficiency

ORPHA:156Disease
Autosomal recessive

Carnitine palmitoyltransferase II deficiency

ORPHA:157Disease
Autosomal recessive

Carnitine-acylcarnitine translocase deficiency

ORPHA:159Disease
Autosomal recessive

Carotid web

ORPHA:698260Disease
Not applicable

Cartilage-hair hypoplasia

ORPHA:175Disease
Autosomal recessive

Carvajal syndrome

ORPHA:65282Disease
Autosomal dominant, Autosomal recessive

Castleman disease

ORPHA:160Disease
Not applicable

Cat-scratch disease

ORPHA:50839Disease
Not applicable

Cataract-ataxia-deafness syndrome

ORPHA:1368Disease
Autosomal recessive

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

ORPHA:436174Disease
Autosomal recessive

Catastrophic antiphospholipid syndrome

ORPHA:464343Disease
Not applicable

Catecholaminergic polymorphic ventricular tachycardia

ORPHA:3286Disease
Autosomal dominant, Autosomal recessive

Cathepsin A-related arteriopathy-strokes-leukoencephalopathy

ORPHA:575553Disease
Autosomal dominant

Cavitary myiasis

ORPHA:165958Disease
Not applicable

Celiac artery compression syndrome

ORPHA:293208Disease
Not applicable

Celiac disease-epilepsy-cerebral calcification syndrome

ORPHA:1459Disease
Not applicable

Central areolar choroidal dystrophy

ORPHA:75377Disease
Autosomal dominant