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7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 1,772 заболеваний (Мальф.) Қалпына келтіру

Congenital subglottic stenosis

ORPHA:141121Мальф.

Congenital vertebral-cardiac-renal anomalies syndrome

ORPHA:521438Мальф.
Autosomal recessive

Congenitally short costocoracoid ligament

ORPHA:2391Мальф.
Autosomal dominant

Cono-spondylar dysplasia

ORPHA:420794Мальф.
Autosomal recessive

Contractures-developmental delay-Pierre Robin syndrome

ORPHA:436003Мальф.
Unknown

Contractures-ectodermal dysplasia-cleft lip/palate syndrome

ORPHA:1484Мальф.
Autosomal recessive, X-linked recessive

Contractures-webbed neck-micrognathia-hypoplastic nipples syndrome

ORPHA:314002Мальф.
No data available

Cooks syndrome

ORPHA:1487Мальф.
Autosomal dominant

Cooper-Jabs syndrome

ORPHA:1488Мальф.
Autosomal recessive

Corneal dystrophy-perceptive deafness syndrome

ORPHA:1490Мальф.
Autosomal recessive

Cornelia de Lange syndrome

ORPHA:199Мальф.
Autosomal dominant, Not applicable, X-linked recessive

Corneodermatoosseous syndrome

ORPHA:3194Мальф.
Autosomal dominant

Corpus callosum agenesis-abnormal genitalia syndrome

ORPHA:2508Мальф.
X-linked recessive

Corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome

ORPHA:52055Мальф.
X-linked recessive

Corpus callosum agenesis-macrocephaly-hypertelorism syndrome

ORPHA:459074Мальф.
Unknown

Cortical blindness-intellectual disability-polydactyly syndrome

ORPHA:1389Мальф.
Autosomal recessive

Costello syndrome

ORPHA:3071Мальф.
Autosomal dominant, Not applicable

Coxoauricular syndrome

ORPHA:1508Мальф.
Unknown

Crane-Heise syndrome

ORPHA:1512Мальф.
Autosomal recessive

Cranio-osteoarthropathy

ORPHA:1525Мальф.
Autosomal recessive

Craniodiaphyseal dysplasia

ORPHA:1513Мальф.
Autosomal dominant, Autosomal recessive, Not applicable

Craniodigital-intellectual disability syndrome

ORPHA:1514Мальф.
Autosomal recessive, X-linked recessive

Cranioectodermal dysplasia

ORPHA:1515Мальф.
Autosomal recessive

Craniofacial conodysplasia

ORPHA:85168Мальф.
Autosomal dominant