MEDLIB
База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

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

Moderate hemophilia B

ORPHA:169796Клин. подт.
X-linked recessive

Moderate multiminicore disease with hand involvement

ORPHA:178145Клин. подт.
Autosomal dominant

Moderately-differentiated thymic neuroendocrine carcinoma

ORPHA:263335Гист. подт.
Not applicable

Moebius syndrome

ORPHA:570Заболевание
Autosomal dominant

Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome

ORPHA:2560Порок
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:2565Порок
X-linked dominant

Monosomy 13q14 syndrome

ORPHA:1587Порок
Not applicable

Monosomy 13q34 syndrome

ORPHA:96168Порок
Not applicable

Monosomy 18p syndrome

ORPHA:1598Заболевание
Autosomal dominant

Monosomy 18q syndrome

ORPHA:1600Порок
Autosomal dominant

Monosomy 22 syndrome

ORPHA:96123Порок

Monosomy 5p syndrome

ORPHA:281Порок
Not applicable, Unknown

Monosomy 9p syndrome

ORPHA:261112Порок

Monosomy 9q22.3 syndrome

ORPHA:77301Порок
Not applicable, Unknown

Monosomy X syndrome

ORPHA:99226Этиол. подт.
Not applicable

Monostotic fibrous dysplasia

ORPHA:93277Клин. подт.
Not applicable

Morgagni-Stewart-Morel syndrome

ORPHA:77296Порок
Autosomal dominant, X-linked recessive

Morning glory disc anomaly

ORPHA:35737Морф.

Morvan syndrome

ORPHA:83467Заболевание