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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Myelodysplastic syndrome

ORPHA:52688Клин. гр.

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

ORPHA:86841Заболевание
Not applicable

Myelodysplastic/myeloproliferative disease

ORPHA:98275Клин. гр.

Myeloid sarcoma

ORPHA:86850Заболевание
Not applicable

Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement

ORPHA:168953Заболевание

Myeloid/lymphoid neoplasm associated with JAK2 rearrangement

ORPHA:589542Заболевание

Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement

ORPHA:168947Заболевание

Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement

ORPHA:168950Заболевание

Myeloperoxidase deficiency

ORPHA:2587Заболевание
Autosomal recessive

Myeloproliferative neoplasm

ORPHA:98274Клин. гр.

Myhre syndrome

ORPHA:2588Порок
Autosomal dominant

Myoclonic epilepsy in non-progressive encephalopathies

ORPHA:86913Порок

Myoclonic epilepsy of infancy

ORPHA:86909Заболевание
Autosomal recessive

Myoclonus-cerebellar ataxia-deafness syndrome

ORPHA:2589Порок
Autosomal dominant

Myoclonus-dystonia syndrome

ORPHA:36899Заболевание
Autosomal dominant, Not applicable

Myofibrillar myopathy

ORPHA:593Кат.
Autosomal dominant, Autosomal recessive

Myopathic Ehlers-Danlos syndrome

ORPHA:536516Заболевание
Autosomal dominant, Autosomal recessive

Myopathic intestinal pseudoobstruction

ORPHA:104077Этиол. подт.
Unknown

Myopathy and diabetes mellitus

ORPHA:2596Заболевание
Mitochondrial inheritance

Myosclerosis

ORPHA:289380Заболевание
Autosomal recessive

Myosin storage myopathy

ORPHA:53698Заболевание
Autosomal dominant, Autosomal recessive

Myospherulosis

ORPHA:306553Заболевание
Not applicable

Myotonia fluctuans

ORPHA:99734Заболевание
Autosomal dominant

Myotonia permanens

ORPHA:99735Заболевание
Autosomal dominant