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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

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

Brachydactyly type E

ORPHA:93387Мальф.
Autosomal dominant

Brachydactyly-arterial hypertension syndrome

ORPHA:1276Мальф.
Autosomal dominant

Brachydactyly-elbow wrist dysplasia syndrome

ORPHA:1275Мальф.
Autosomal dominant

Brachydactyly-long thumb syndrome

ORPHA:2946Мальф.
Autosomal dominant

Brachydactyly-mesomelia-intellectual disability-heart defects syndrome

ORPHA:1277Мальф.

Brachydactyly-nystagmus-cerebellar ataxia syndrome

ORPHA:1246Мальф.
Unknown

Brachydactyly-preaxial hallux varus syndrome

ORPHA:1278Мальф.
Autosomal dominant

Brachydactyly-short stature-retinitis pigmentosa syndrome

ORPHA:166035Мальф.
Autosomal recessive

Brachydactyly-syndactyly, Zhao type

ORPHA:93409Мальф.
Autosomal dominant

Brachymorphism-onychodysplasia-dysphalangism syndrome

ORPHA:1292Мальф.
Autosomal dominant

Brachyolmia, Maroteaux type

ORPHA:93302Мальф.
Autosomal recessive

Brachyolmia-amelogenesis imperfecta syndrome

ORPHA:2899Мальф.
Autosomal recessive

Brachytelephalangic chondrodysplasia punctata

ORPHA:79345Мальф.
X-linked recessive

Brachytelephalangy-dysmorphism-Kallmann syndrome

ORPHA:1295Мальф.
Autosomal dominant

Braddock syndrome

ORPHA:52047Мальф.
Autosomal recessive

Brain abnormalities-severe developmental delay-facial dysmorphism-intellectual disability syndrome

ORPHA:664410Мальф.
Autosomal dominant, Not applicable

Brain malformation-congenital heart disease-postaxial polydactyly syndrome

ORPHA:75389Мальф.
Unknown

Branchio-oculo-facial syndrome

ORPHA:1297Мальф.
Autosomal dominant

Branchiogenic deafness syndrome

ORPHA:50815Мальф.
Autosomal dominant

Branchiootic syndrome

ORPHA:52429Мальф.
Autosomal dominant

Branchioskeletogenital syndrome

ORPHA:1299Мальф.
Autosomal recessive, X-linked dominant

Bronchopulmonary dysplasia

ORPHA:70589Мальф.
Not applicable

Bruck syndrome

ORPHA:2771Мальф.
Autosomal recessive

Burn-McKeown syndrome

ORPHA:1200Мальф.
Autosomal recessive