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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Myelodysplastic syndrome

ORPHA:52688Clin. grp.

Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality

ORPHA:86841Disease
Not applicable

Myelodysplastic/myeloproliferative disease

ORPHA:98275Clin. grp.

Myeloid sarcoma

ORPHA:86850Disease
Not applicable

Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement

ORPHA:168953Disease

Myeloid/lymphoid neoplasm associated with JAK2 rearrangement

ORPHA:589542Disease

Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement

ORPHA:168947Disease

Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement

ORPHA:168950Disease

Myeloperoxidase deficiency

ORPHA:2587Disease
Autosomal recessive

Myeloproliferative neoplasm

ORPHA:98274Clin. grp.

Myhre syndrome

ORPHA:2588Malform.
Autosomal dominant

Myoclonic epilepsy in non-progressive encephalopathies

ORPHA:86913Malform.

Myoclonic epilepsy of infancy

ORPHA:86909Disease
Autosomal recessive

Myoclonus-cerebellar ataxia-deafness syndrome

ORPHA:2589Malform.
Autosomal dominant

Myoclonus-dystonia syndrome

ORPHA:36899Disease
Autosomal dominant, Not applicable

Myofibrillar myopathy

ORPHA:593Cat.
Autosomal dominant, Autosomal recessive

Myopathic Ehlers-Danlos syndrome

ORPHA:536516Disease
Autosomal dominant, Autosomal recessive

Myopathic intestinal pseudoobstruction

ORPHA:104077Etio. sub.
Unknown

Myopathy and diabetes mellitus

ORPHA:2596Disease
Mitochondrial inheritance

Myosclerosis

ORPHA:289380Disease
Autosomal recessive

Myosin storage myopathy

ORPHA:53698Disease
Autosomal dominant, Autosomal recessive

Myospherulosis

ORPHA:306553Disease
Not applicable

Myotonia fluctuans

ORPHA:99734Disease
Autosomal dominant

Myotonia permanens

ORPHA:99735Disease
Autosomal dominant