Редкие (орфанные) заболевания
Полная база данных 7,547 заболеваний с генетикой, фенотипами, эпидемиологией, лекарствами и клиническими исследованиями.
Cryptomicrotia-brachydactyly-excess fingertip arch syndrome
Autosomal dominant
Neonatal
Cryptorchidism-arachnodactyly-intellectual disability syndrome
Infancy, Neonatal
Cryptosporidiosis
Not applicable
Curly hair-acral keratoderma-caries syndrome
Adolescent, Childhood
Currarino syndrome
Autosomal dominant, Not applicable
All ages
Curry-Jones syndrome
Not applicable
Neonatal
Cushing disease
Not applicable
Adult
Cushing syndrome due to bilateral macronodular adrenocortical disease
Autosomal dominant, Not applicable
All ages
Cushing syndrome due to ectopic ACTH secretion
Not applicable
Adult, Elderly
Cutaneous collagenous vasculopathy
Not applicable
Adult
Cutaneous larva migrans
Not applicable
All ages
Cutaneous mastocytoma
Not applicable
All ages
Cutaneous mastocytosis
Not applicable
Childhood
Cutaneous mastocytosis-deafness-microtia syndrome
Autosomal recessive
Infancy, Neonatal
Cutaneous neuroendocrine carcinoma
Not applicable
Adult, Elderly
Cutaneous photosensitivity-lethal colitis syndrome
Autosomal recessive
Infancy, Neonatal
Cutaneous polyarteritis nodosa
Not applicable
Cutaneous pseudolymphoma
Not applicable
Adult, Elderly
Cutaneous small vessel vasculitis
Not applicable
All ages
Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome
Autosomal dominant
Antenatal, Neonatal
Cutis laxa
Autosomal dominant, Autosomal recessive, Not applicable, X-linked recessive
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies
Autosomal recessive
Neonatal
Cutis laxa-Marfanoid syndrome
Infancy, Neonatal
Cutis marmorata telangiectatica congenita
Not applicable
Neonatal