MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Cryptomicrotia-brachydactyly-excess fingertip arch syndrome

ORPHA:1547Malf.
Autosomal dominant

Cryptorchidism-arachnodactyly-intellectual disability syndrome

ORPHA:1548Malf.

Cryptosporidiosis

ORPHA:697096Kr.
Not applicable

Curly hair-acral keratoderma-caries syndrome

ORPHA:307766Kr.

Currarino syndrome

ORPHA:1552Malf.
Autosomal dominant, Not applicable

Curry-Jones syndrome

ORPHA:1553Malf.
Not applicable

Cushing disease

ORPHA:96253Kr.
Not applicable

Cushing syndrome due to bilateral macronodular adrenocortical disease

ORPHA:189427Kr.
Autosomal dominant, Not applicable

Cushing syndrome due to ectopic ACTH secretion

ORPHA:99889Kr.
Not applicable

Cutaneous collagenous vasculopathy

ORPHA:280779Kr.
Not applicable

Cutaneous larva migrans

ORPHA:423717Kr.
Not applicable

Cutaneous mastocytoma

ORPHA:79455Kr.
Not applicable

Cutaneous mastocytosis

ORPHA:66646Kl. gruppe
Not applicable

Cutaneous mastocytosis-deafness-microtia syndrome

ORPHA:2135Malf.
Autosomal recessive

Cutaneous neuroendocrine carcinoma

ORPHA:79140Kr.
Not applicable

Cutaneous photosensitivity-lethal colitis syndrome

ORPHA:2881Kr.
Autosomal recessive

Cutaneous polyarteritis nodosa

ORPHA:439729Kl. subt.
Not applicable

Cutaneous pseudolymphoma

ORPHA:451607Kr.
Not applicable

Cutaneous small vessel vasculitis

ORPHA:889Kr.
Not applicable

Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome

ORPHA:1555Malf.
Autosomal dominant

Cutis laxa

ORPHA:209Kl. gruppe
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive

Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies

ORPHA:221145Malf.
Autosomal recessive

Cutis laxa-Marfanoid syndrome

ORPHA:171719Malf.

Cutis marmorata telangiectatica congenita

ORPHA:1556Malf.
Not applicable