MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Мальформация
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Мальформация

Cryptosporidiosis

ORPHA:697096Заболевание
Not applicable

Curly hair-acral keratoderma-caries syndrome

ORPHA:307766Заболевание

Currarino syndrome

ORPHA:1552Мальформация
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Мальформация
Not applicable

Cushing disease

ORPHA:96253Заболевание
Not applicable

Cushing syndrome due to bilateral macronodular adrenocortical disease

ORPHA:189427Заболевание
Autosomal dominant, Not applicable

Cushing syndrome due to ectopic ACTH secretion

ORPHA:99889Заболевание
Not applicable

Cutaneous collagenous vasculopathy

ORPHA:280779Заболевание
Not applicable

Cutaneous larva migrans

ORPHA:423717Заболевание
Not applicable

Cutaneous mastocytoma

ORPHA:79455Заболевание
Not applicable

Cutaneous mastocytosis

ORPHA:66646Клин. группа
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Мальформация
Autosomal recessive

Cutaneous neuroendocrine carcinoma

ORPHA:79140Заболевание
Not applicable

Cutaneous photosensitivity-lethal colitis syndrome

ORPHA:2881Заболевание
Autosomal recessive

Cutaneous polyarteritis nodosa

ORPHA:439729Клин. подтип
Not applicable

Cutaneous pseudolymphoma

ORPHA:451607Заболевание
Not applicable

Cutaneous small vessel vasculitis

ORPHA:889Заболевание
Not applicable

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Мальформация
Autosomal dominant

Cutis laxa

ORPHA:209Клин. группа
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Мальформация
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Мальформация

Cutis marmorata telangiectatica congenita

ORPHA:1556Мальформация
Not applicable