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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 3,968 заболеваний (Ауру) Қалпына келтіру

Cardiomyopathy-cataract-hip spine disease syndrome

ORPHA:1345Ауру
Autosomal recessive

Cardiomyopathy-hypotonia-lactic acidosis syndrome

ORPHA:91130Ауру
Autosomal recessive

Caribbean parkinsonism

ORPHA:97355Ауру

Carney complex

ORPHA:1359Ауру
Autosomal dominant

Carney complex-trismus-pseudocamptodactyly syndrome

ORPHA:319340Ауру
Not applicable

Carney triad

ORPHA:139411Ауру

Carney-Stratakis syndrome

ORPHA:97286Ауру
Autosomal dominant

Carnitine palmitoyl transferase 1A deficiency

ORPHA:156Ауру
Autosomal recessive

Carnitine palmitoyltransferase II deficiency

ORPHA:157Ауру
Autosomal recessive

Carnitine-acylcarnitine translocase deficiency

ORPHA:159Ауру
Autosomal recessive

Carotid web

ORPHA:698260Ауру
Not applicable

Cartilage-hair hypoplasia

ORPHA:175Ауру
Autosomal recessive

Carvajal syndrome

ORPHA:65282Ауру
Autosomal dominant, Autosomal recessive

Castleman disease

ORPHA:160Ауру
Not applicable

Cat-scratch disease

ORPHA:50839Ауру
Not applicable

Cataract-ataxia-deafness syndrome

ORPHA:1368Ауру
Autosomal recessive

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

ORPHA:436174Ауру
Autosomal recessive

Catastrophic antiphospholipid syndrome

ORPHA:464343Ауру
Not applicable

Catecholaminergic polymorphic ventricular tachycardia

ORPHA:3286Ауру
Autosomal dominant, Autosomal recessive

Cathepsin A-related arteriopathy-strokes-leukoencephalopathy

ORPHA:575553Ауру
Autosomal dominant

Cavitary myiasis

ORPHA:165958Ауру
Not applicable

Celiac artery compression syndrome

ORPHA:293208Ауру
Not applicable

Celiac disease-epilepsy-cerebral calcification syndrome

ORPHA:1459Ауру
Not applicable

Central areolar choroidal dystrophy

ORPHA:75377Ауру
Autosomal dominant