MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Moderate hemophilia B

ORPHA:169796Клин. подтип
X-linked recessive

Moderate multiminicore disease with hand involvement

ORPHA:178145Клин. подтип
Autosomal dominant

Moderately-differentiated thymic neuroendocrine carcinoma

ORPHA:263335Гист. подтип
Not applicable

Moebius syndrome

ORPHA:570Заболевание
Autosomal dominant

Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome

ORPHA:2560Мальформация
Not applicable

Mohr-Tranebjaerg syndrome

ORPHA:52368Заболевание
X-linked recessive

Monilethrix

ORPHA:573Заболевание
Autosomal dominant, Autosomal recessive

Monoamine oxidase A deficiency

ORPHA:3057Заболевание
X-linked recessive

Monoclonal mast cell activation syndrome

ORPHA:529468Заболевание

Monomelic amyotrophy

ORPHA:65684Заболевание
Unknown

Mononen-Karnes-Senac syndrome

ORPHA:2565Мальформация
X-linked dominant

Monosomy 13q14 syndrome

ORPHA:1587Мальформация
Not applicable

Monosomy 13q34 syndrome

ORPHA:96168Мальформация
Not applicable

Monosomy 18p syndrome

ORPHA:1598Заболевание
Autosomal dominant

Monosomy 18q syndrome

ORPHA:1600Мальформация
Autosomal dominant

Monosomy 22 syndrome

ORPHA:96123Мальформация

Monosomy 5p syndrome

ORPHA:281Мальформация
Not applicable, Unknown

Monosomy 9p syndrome

ORPHA:261112Мальформация

Monosomy 9q22.3 syndrome

ORPHA:77301Мальформация
Not applicable, Unknown

Monosomy X syndrome

ORPHA:99226Этиол. подтип
Not applicable

Monostotic fibrous dysplasia

ORPHA:93277Клин. подтип
Not applicable

Morgagni-Stewart-Morel syndrome

ORPHA:77296Мальформация
Autosomal dominant, X-linked recessive

Morning glory disc anomaly

ORPHA:35737Морф. аномалия

Morvan syndrome

ORPHA:83467Заболевание