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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

ANE syndrome

ORPHA:157954Disease
Autosomal recessive

ANK3-related intellectual disability-sleep disturbance syndrome

ORPHA:356996Disease
Autosomal recessive

AREDYLD syndrome

ORPHA:1133Malform.
Autosomal recessive

ARX-related encephalopathy-brain malformation spectrum

ORPHA:423655Clin. grp.

ATP13A2-related parkinsonism

ORPHA:514980Clin. grp.

ATP6AP1-CDG

ORPHA:692790Disease
X-linked recessive

ATTRV122I amyloidosis

ORPHA:85451Clin. sub.
Autosomal dominant

ATTRV30M amyloidosis

ORPHA:85447Clin. sub.
Autosomal dominant

AXIN2-related polyposis

ORPHA:401911Disease
Autosomal dominant

Aarskog-Scott syndrome

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

Aase-Smith syndrome type 1

ORPHA:916Malform.
Autosomal dominant

Abetalipoproteinemia

ORPHA:14Disease
Autosomal recessive

Ablepharon macrostomia syndrome

ORPHA:920Malform.
Autosomal dominant

Abnormal origin of right or left pulmonary artery from the aorta

ORPHA:99050Morph.

Abruzzo-Erickson syndrome

ORPHA:921Malform.
X-linked recessive

Absence deformity of leg-cataract syndrome

ORPHA:2310Malform.

Absence of fingerprints-congenital milia syndrome

ORPHA:1658Disease
Autosomal dominant

Absence of the pulmonary artery

ORPHA:980Morph.
Not applicable

Absent radius-anogenital anomalies syndrome

ORPHA:3016Malform.

Absent thumb-short stature-immunodeficiency syndrome

ORPHA:2951Malform.
Unknown

Absent tibia-polydactyly-arachnoid cyst syndrome

ORPHA:3328Malform.
Unknown

Acalvaria

ORPHA:945Malform.
Not applicable

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

ORPHA:90301Disease

Acatalasemia

ORPHA:926Disease
Autosomal recessive