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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Malform.
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Malform.

Cryptosporidiosis

ORPHA:697096Disease
Not applicable

Curly hair-acral keratoderma-caries syndrome

ORPHA:307766Disease

Currarino syndrome

ORPHA:1552Malform.
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Malform.
Not applicable

Cushing disease

ORPHA:96253Disease
Not applicable

Cushing syndrome due to bilateral macronodular adrenocortical disease

ORPHA:189427Disease
Autosomal dominant, Not applicable

Cushing syndrome due to ectopic ACTH secretion

ORPHA:99889Disease
Not applicable

Cutaneous collagenous vasculopathy

ORPHA:280779Disease
Not applicable

Cutaneous larva migrans

ORPHA:423717Disease
Not applicable

Cutaneous mastocytoma

ORPHA:79455Disease
Not applicable

Cutaneous mastocytosis

ORPHA:66646Clin. grp.
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Malform.
Autosomal recessive

Cutaneous neuroendocrine carcinoma

ORPHA:79140Disease
Not applicable

Cutaneous photosensitivity-lethal colitis syndrome

ORPHA:2881Disease
Autosomal recessive

Cutaneous polyarteritis nodosa

ORPHA:439729Clin. sub.
Not applicable

Cutaneous pseudolymphoma

ORPHA:451607Disease
Not applicable

Cutaneous small vessel vasculitis

ORPHA:889Disease
Not applicable

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Malform.
Autosomal dominant

Cutis laxa

ORPHA:209Clin. grp.
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Malform.
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Malform.

Cutis marmorata telangiectatica congenita

ORPHA:1556Malform.
Not applicable