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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

Heart defects-limb shortening syndrome

ORPHA:1354Мальф.
Autosomal recessive

Heart-hand syndrome type 2

ORPHA:1350Мальф.

Heart-hand syndrome type 3

ORPHA:1342Мальф.

Heart-hand syndrome, Slovenian type

ORPHA:168796Мальф.
Autosomal dominant

Helsmoortel-Van der Aa syndrome

ORPHA:404448Мальф.
Unknown

Hemifacial hyperplasia

ORPHA:141145Мальф.
Not applicable

Hemifacial myohyperplasia

ORPHA:141148Мальф.

Hemihyperplasia-multiple lipomatosis syndrome

ORPHA:276280Мальф.
Not applicable

Hemimegalencephaly

ORPHA:99802Мальф.
Not applicable

Hennekam syndrome

ORPHA:2136Мальф.
Autosomal recessive

Hepatic arteriovenous malformation

ORPHA:693846Мальф.
Not applicable

Hepatic fibrosis-renal cysts-intellectual disability syndrome

ORPHA:2031Мальф.

Hereditary gingival fibromatosis

ORPHA:2024Мальф.
Autosomal dominant

Hereditary mucoepithelial dysplasia

ORPHA:1839Мальф.
Autosomal dominant

Hereditary neuropathy with liability to pressure palsies

ORPHA:640Мальф.
Autosomal dominant

Hereditary renal hypouricemia

ORPHA:94088Мальф.
Autosomal recessive

Hernández-Aguirre Negrete syndrome

ORPHA:2139Мальф.
Autosomal recessive

Hidrotic ectodermal dysplasia, Christianson-Fourie type

ORPHA:1808Мальф.
Autosomal dominant

Hidrotic ectodermal dysplasia, Halal type

ORPHA:1809Мальф.
Autosomal recessive

Hirschsprung disease-deafness-polydactyly syndrome

ORPHA:2155Мальф.
Autosomal recessive

Hirschsprung disease-ganglioneuroblastoma syndrome

ORPHA:2151Мальф.

Hirschsprung disease-nail hypoplasia-dysmorphism syndrome

ORPHA:2153Мальф.
Autosomal recessive

Hirschsprung disease-type D brachydactyly syndrome

ORPHA:2150Мальф.

Holoprosencephaly

ORPHA:2162Мальф.
Autosomal recessive, Multigenic/multifactorial, Not applicable, Oligogenic, X-linked dominant