MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Myelodysplastic syndrome

ORPHA:52688Клин. группа

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

ORPHA:86841Заболевание
Not applicable

Myelodysplastic/myeloproliferative disease

ORPHA:98275Клин. группа

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. группа

Myhre syndrome

ORPHA:2588Мальформация
Autosomal dominant

Myoclonic epilepsy in non-progressive encephalopathies

ORPHA:86913Мальформация

Myoclonic epilepsy of infancy

ORPHA:86909Заболевание
Autosomal recessive

Myoclonus-cerebellar ataxia-deafness syndrome

ORPHA:2589Мальформация
Autosomal dominant

Myoclonus-dystonia syndrome

ORPHA:36899Заболевание
Autosomal dominant, Not applicable

Myofibrillar myopathy

ORPHA:593Категория
Autosomal dominant, Autosomal recessive

Myopathic Ehlers-Danlos syndrome

ORPHA:536516Заболевание
Autosomal dominant, Autosomal recessive

Myopathic intestinal pseudoobstruction

ORPHA:104077Этиол. подтип
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