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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome due to TPP2 deficiency

ORPHA:444463Ауру
Autosomal recessive

Autoimmune hepatitis

ORPHA:2137Ауру
Not applicable

Autoimmune hepatitis type 1

ORPHA:563576Клин. под.

Autoimmune hepatitis type 2

ORPHA:563581Клин. под.

Autoimmune hypoparathyroidism

ORPHA:36913Ауру
Not applicable

Autoimmune interstitial lung disease-arthritis syndrome

ORPHA:444092Ауру
Autosomal dominant

Autoimmune limbic encephalitis

ORPHA:623615Ауру

Autoimmune lymphoproliferative syndrome

ORPHA:3261Ауру
Autosomal dominant, Autosomal recessive

Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency

ORPHA:436159Ауру
Autosomal dominant

Autoimmune lymphoproliferative syndrome-recurrent viral infections due to CASP8 deficiency

ORPHA:275517Ауру
Autosomal recessive

Autoimmune pancreatitis

ORPHA:103919Клин. топ
Not applicable

Autoimmune pancreatitis type 1

ORPHA:280302Клин. под.
Not applicable

Autoimmune pancreatitis type 2

ORPHA:280315Ауру
Not applicable

Autoimmune polyendocrinopathy type 1

ORPHA:3453Ауру
Autosomal recessive

Autoimmune polyendocrinopathy type 2

ORPHA:3143Ауру

Autoimmune polyendocrinopathy type 3

ORPHA:227982Ауру
Multigenic/multifactorial

Autoimmune polyendocrinopathy type 4

ORPHA:227990Ауру
Multigenic/multifactorial

Autoimmune pulmonary alveolar proteinosis

ORPHA:747Ауру
Multigenic/multifactorial, Not applicable

Autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation

ORPHA:324530Ауру
Autosomal dominant

Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis

ORPHA:329173Ауру
Autosomal recessive

Autosomal dominant ACTN2-related distal myopathy

ORPHA:708133Ауру
Autosomal dominant

Autosomal dominant Alport syndrome

ORPHA:88918Клин. под.
Autosomal dominant

Autosomal dominant Charcot-Marie-Tooth disease type 2

ORPHA:64746Клин. топ
Autosomal dominant

Autosomal dominant Charcot-Marie-Tooth disease type 2 due to DGAT2 mutation

ORPHA:487814Ауру
Autosomal dominant