MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4,552Gene
8,700Phänotypen

Mucopolysaccharidosis type 2, attenuated form

ORPHA:217093Kl. subt.
X-linked recessive

Mucopolysaccharidosis type 2, severe form

ORPHA:217085Kl. subt.
X-linked recessive

Mucopolysaccharidosis type 3

ORPHA:581Kr.
Autosomal recessive

Mucopolysaccharidosis type 4

ORPHA:582Kr.
Autosomal recessive

Mucopolysaccharidosis type 4A

ORPHA:309297Kl. subt.
Autosomal recessive

Mucopolysaccharidosis type 4B

ORPHA:309310Kl. subt.
Autosomal recessive

Mucopolysaccharidosis type 6

ORPHA:583Kr.
Autosomal recessive

Mucopolysaccharidosis type 6, rapidly progressing

ORPHA:276212Kl. subt.
Autosomal recessive

Mucopolysaccharidosis type 6, slowly progressing

ORPHA:276223Kl. subt.
Autosomal recessive

Mucopolysaccharidosis type 7

ORPHA:584Kr.
Autosomal recessive

Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders

ORPHA:505248Malf.
Autosomal recessive

Mucous membrane pemphigoid

ORPHA:46486Kr.
Not applicable

Mueller-Weiss syndrome

ORPHA:566943Kr.

Muenke syndrome

ORPHA:53271Malf.
Autosomal dominant

Mulibrey nanism

ORPHA:2576Malf.
Autosomal recessive

Multicentric carpo-tarsal osteolysis with or without nephropathy

ORPHA:2774Malf.
Autosomal dominant

Multicentric osteolysis-nodulosis-arthropathy spectrum

ORPHA:371428Kr.
Autosomal recessive

Multicentric reticulohistiocytosis

ORPHA:139436Kr.
Not applicable

Multicystic dysplastic kidney

ORPHA:1851Morph.
Not applicable

Multifocal atrial tachycardia

ORPHA:3282Kr.
Not applicable

Multifocal infantile hemangioma with extracutenous involvement

ORPHA:2123Kr.
Not applicable

Multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome

ORPHA:464321Kr.
Not applicable

Multifocal motor neuropathy

ORPHA:641Kr.
Unknown

Multifocal pattern dystrophy simulating fundus flavimaculatus

ORPHA:99003Kr.
Autosomal dominant