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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Mucopolysaccharidosis type 2, attenuated form

ORPHA:217093Clin. sub.
X-linked recessive

Mucopolysaccharidosis type 2, severe form

ORPHA:217085Clin. sub.
X-linked recessive

Mucopolysaccharidosis type 3

ORPHA:581Disease
Autosomal recessive

Mucopolysaccharidosis type 4

ORPHA:582Disease
Autosomal recessive

Mucopolysaccharidosis type 4A

ORPHA:309297Clin. sub.
Autosomal recessive

Mucopolysaccharidosis type 4B

ORPHA:309310Clin. sub.
Autosomal recessive

Mucopolysaccharidosis type 6

ORPHA:583Disease
Autosomal recessive

Mucopolysaccharidosis type 6, rapidly progressing

ORPHA:276212Clin. sub.
Autosomal recessive

Mucopolysaccharidosis type 6, slowly progressing

ORPHA:276223Clin. sub.
Autosomal recessive

Mucopolysaccharidosis type 7

ORPHA:584Disease
Autosomal recessive

Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders

ORPHA:505248Malform.
Autosomal recessive

Mucous membrane pemphigoid

ORPHA:46486Disease
Not applicable

Mueller-Weiss syndrome

ORPHA:566943Disease

Muenke syndrome

ORPHA:53271Malform.
Autosomal dominant

Mulibrey nanism

ORPHA:2576Malform.
Autosomal recessive

Multicentric carpo-tarsal osteolysis with or without nephropathy

ORPHA:2774Malform.
Autosomal dominant

Multicentric osteolysis-nodulosis-arthropathy spectrum

ORPHA:371428Disease
Autosomal recessive

Multicentric reticulohistiocytosis

ORPHA:139436Disease
Not applicable

Multicystic dysplastic kidney

ORPHA:1851Morph.
Not applicable

Multifocal atrial tachycardia

ORPHA:3282Disease
Not applicable

Multifocal infantile hemangioma with extracutenous involvement

ORPHA:2123Disease
Not applicable

Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome

ORPHA:464321Disease
Not applicable

Multifocal motor neuropathy

ORPHA:641Disease
Unknown

Multifocal pattern dystrophy simulating fundus flavimaculatus

ORPHA:99003Disease
Autosomal dominant