MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы
Найдено 3,968 заболеваний (Disease) Сброс

Adenylosuccinate lyase deficiency

ORPHA:46Disease
Autosomal recessive

Adenylosuccinate synthetase-like 1-related distal myopathy

ORPHA:482601Disease
Autosomal recessive

Adiposis dolorosa

ORPHA:36397Disease
Autosomal dominant, Not applicable

Adrenocortical carcinoma

ORPHA:1501Disease
Not applicable

Adrenocortical carcinoma with pure aldosterone hypersecretion

ORPHA:231625Disease
Not applicable

Adrenomyodystrophy

ORPHA:977Disease
Unknown

Adult Refsum disease

ORPHA:773Disease
Autosomal recessive

Adult T-cell leukemia/lymphoma

ORPHA:86875Disease
Multigenic/multifactorial, Not applicable

Adult acute respiratory distress syndrome

ORPHA:70578Disease
Not applicable

Adult familial nephronophthisis-spastic quadriparesia syndrome

ORPHA:2666Disease
Unknown

Adult hepatocellular carcinoma

ORPHA:210159Disease
Not applicable

Adult idiopathic neutropenia

ORPHA:2688Disease
Not applicable

Adult-onset Still disease

ORPHA:829Disease
Not applicable

Adult-onset autosomal dominant leukodystrophy

ORPHA:99027Disease
Autosomal dominant

Adult-onset autosomal recessive cerebellar ataxia

ORPHA:284289Disease
Autosomal recessive

Adult-onset autosomal recessive sideroblastic anemia

ORPHA:255132Disease
Autosomal recessive

Adult-onset cervical dystonia, DYT23 type

ORPHA:420492Disease
Autosomal dominant

Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy

ORPHA:329336Disease
Autosomal dominant, Mitochondrial inheritance

Adult-onset common variable immunodeficiency due to BAFF-receptor deficiency

ORPHA:696925Disease
Autosomal recessive

Adult-onset distal myopathy due to VCP mutation

ORPHA:329478Disease
Autosomal dominant

Adult-onset dystonia-parkinsonism

ORPHA:199351Disease
Autosomal recessive

Adult-onset foveomacular vitelliform dystrophy

ORPHA:99000Disease
Autosomal dominant, Not applicable

Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies

ORPHA:306431Disease
Not applicable

Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia

ORPHA:313808Disease
Autosomal dominant