MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Mounier-Kühn syndrome

ORPHA:3347Clinical syndrome
Not applicable

Mowat-Wilson syndrome

ORPHA:2152Мальформация
Autosomal dominant

Mowat-Wilson syndrome due to a ZEB2 point mutation

ORPHA:261552Этиол. подтип
Autosomal dominant

Mowat-Wilson syndrome due to monosomy 2q22

ORPHA:261537Этиол. подтип

Moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome

ORPHA:280679Заболевание
X-linked recessive

Moyamoya disease

ORPHA:2573Заболевание
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive

Moyamoya disease with early-onset achalasia

ORPHA:401945Заболевание
Autosomal recessive

Mu-heavy chain disease

ORPHA:100024Клин. подтип

Mucinous adenocarcinoma of ovary

ORPHA:398961Заболевание

Mucinous adenocarcinoma of the appendix

ORPHA:391723Заболевание

Mucinous cystadenocarcinoma of the pancreas

ORPHA:424053Заболевание
Not applicable

Mucinous cystadenoma of childhood

ORPHA:563671Гист. подтип

Mucinous tubular and spindle cell renal carcinoma

ORPHA:319322Заболевание

Muckle-Wells syndrome

ORPHA:575Заболевание
Autosomal dominant

Mucocutaneous venous malformations

ORPHA:2451Мальформация
Autosomal dominant

Mucolipidosis type II

ORPHA:576Заболевание
Autosomal recessive

Mucolipidosis type III

ORPHA:577Заболевание
Autosomal recessive

Mucolipidosis type III alpha/beta

ORPHA:423461Клин. подтип
Autosomal recessive

Mucolipidosis type III gamma

ORPHA:423470Клин. подтип
Autosomal recessive

Mucolipidosis type IV

ORPHA:578Заболевание
Autosomal recessive

Mucopolysaccharidosis

ORPHA:79213Категория

Mucopolysaccharidosis type 1

ORPHA:579Заболевание
Autosomal recessive

Mucopolysaccharidosis type 10

ORPHA:662216Заболевание
Autosomal recessive

Mucopolysaccharidosis type 2

ORPHA:580Заболевание
X-linked recessive