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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Autosomal recessive spastic paraplegia type 9B

ORPHA:447760Ауру
Autosomal recessive

Autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome

ORPHA:95433Ауру
Autosomal recessive

Autosomal recessive spondylocostal dysostosis

ORPHA:2311Мальф.
Autosomal recessive

Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type

ORPHA:401979Мальф.
Autosomal recessive

Autosomal recessive syndromic cerebellar ataxia

ORPHA:98099Сан.
Autosomal recessive

Autosomal semi-dominant severe lipodystrophic laminopathy

ORPHA:280365Ауру
Semi-dominant

Autosomal spastic paraplegia type 18

ORPHA:209951Ауру
Autosomal dominant, Autosomal recessive

Autosomal spastic paraplegia type 30

ORPHA:101010Ауру
Autosomal dominant, Autosomal recessive

Autosomal spastic paraplegia type 58

ORPHA:397946Ауру
Autosomal dominant, Autosomal recessive

Autosomal spastic paraplegia type 72

ORPHA:401849Ауру
Autosomal dominant, Autosomal recessive

Autosomal systemic lupus erythematosus

ORPHA:300345Ауру
Autosomal dominant, Autosomal recessive

Autosomal thrombocytopenia with normal platelets

ORPHA:168629Этио. под.
Autosomal dominant, Autosomal recessive

Avian influenza

ORPHA:454836Ауру
Not applicable

Axenfeld anomaly

ORPHA:98978Морф.
Autosomal dominant

Axenfeld-Rieger syndrome

ORPHA:782Мальф.
Autosomal dominant

Axial mesodermal dysplasia spectrum

ORPHA:1834Мальф.

Axial spondylometaphyseal dysplasia

ORPHA:168549Ауру
Autosomal recessive

Aymé-Gripp syndrome

ORPHA:1272Мальф.
Autosomal recessive

B-cell chronic lymphocytic leukemia

ORPHA:67038Ауру
Multigenic/multifactorial, Not applicable

B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome

ORPHA:567502Ауру
Autosomal dominant

B-cell non-Hodgkin lymphoma

ORPHA:171915Сан.

B-cell prolymphocytic leukemia

ORPHA:86852Ауру

B-lymphoblastic leukemia/lymphoma with hyperdiploidy

ORPHA:585936Этио. под.

B-lymphoblastic leukemia/lymphoma with hypodiploidy

ORPHA:585942Этио. под.