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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

ANE syndrome

ORPHA:157954Ауру
Autosomal recessive

ANK3-related intellectual disability-sleep disturbance syndrome

ORPHA:356996Ауру
Autosomal recessive

AREDYLD syndrome

ORPHA:1133Мальф.
Autosomal recessive

ARX-related encephalopathy-brain malformation spectrum

ORPHA:423655Клин. топ

ATP13A2-related parkinsonism

ORPHA:514980Клин. топ

ATP6AP1-CDG

ORPHA:692790Ауру
X-linked recessive

ATTRV122I amyloidosis

ORPHA:85451Клин. под.
Autosomal dominant

ATTRV30M amyloidosis

ORPHA:85447Клин. под.
Autosomal dominant

AXIN2-related polyposis

ORPHA:401911Ауру
Autosomal dominant

Aarskog-Scott syndrome

ORPHA:915Мальф.
Autosomal dominant, Autosomal recessive, X-linked recessive

Aase-Smith syndrome type 1

ORPHA:916Мальф.
Autosomal dominant

Abetalipoproteinemia

ORPHA:14Ауру
Autosomal recessive

Ablepharon macrostomia syndrome

ORPHA:920Мальф.
Autosomal dominant

Abnormal origin of right or left pulmonary artery from the aorta

ORPHA:99050Морф.

Abruzzo-Erickson syndrome

ORPHA:921Мальф.
X-linked recessive

Absence deformity of leg-cataract syndrome

ORPHA:2310Мальф.

Absence of fingerprints-congenital milia syndrome

ORPHA:1658Ауру
Autosomal dominant

Absence of the pulmonary artery

ORPHA:980Морф.
Not applicable

Absent radius-anogenital anomalies syndrome

ORPHA:3016Мальф.

Absent thumb-short stature-immunodeficiency syndrome

ORPHA:2951Мальф.
Unknown

Absent tibia-polydactyly-arachnoid cyst syndrome

ORPHA:3328Мальф.
Unknown

Acalvaria

ORPHA:945Мальф.
Not applicable

Acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome

ORPHA:90301Ауру

Acatalasemia

ORPHA:926Ауру
Autosomal recessive