MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Native American myopathy

ORPHA:168572Malf.
Autosomal recessive

Navajo neurohepatopathy

ORPHA:255229Kr.
Autosomal recessive

Naxos disease

ORPHA:34217Kr.
Autosomal recessive

Necrobiosis lipoidica

ORPHA:542592Kr.

Necrobiotic xanthogranuloma

ORPHA:158011Kr.
Not applicable

Necrotizing cellulitis

ORPHA:699678Kl. subt.
Not applicable

Necrotizing enterocolitis

ORPHA:391673Kr.
Not applicable

Necrotizing fasciitis

ORPHA:699697Kl. subt.
Not applicable

Necrotizing myositis

ORPHA:699702Kl. subt.
Not applicable

Necrotizing soft tissue infection

ORPHA:440368Kr.
Not applicable

Nelson syndrome

ORPHA:199244Clinical syndrome

Nemaline myopathy

ORPHA:607Kl. gruppe
Autosomal dominant, Autosomal recessive, Not applicable

Neonatal Marfan syndrome

ORPHA:284979Kr.
Autosomal dominant

Neonatal acute respiratory distress syndrome

ORPHA:217563Kr.
Autosomal recessive

Neonatal adrenoleukodystrophy

ORPHA:44Kr.
Autosomal recessive

Neonatal alloimmune neutropenia

ORPHA:464370Kr.

Neonatal antiphospholipid syndrome

ORPHA:398097Kr.

Neonatal autoimmune hemolytic anemia

ORPHA:398109Kr.

Neonatal compartment syndrome

ORPHA:641829Clinical syndrome

Neonatal dermatomyositis

ORPHA:398117Kr.

Neonatal diabetes mellitus

ORPHA:224Kat.
Autosomal dominant, Autosomal recessive, Not applicable

Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome

ORPHA:79118Kr.
Autosomal recessive

Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

ORPHA:457185Kr.
Autosomal recessive

Neonatal epileptic encephalopathy due to glutaminase deficiency

ORPHA:557064Kr.
Autosomal recessive