MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Narcolepsy type 1

ORPHA:2073Kr.
Unknown

Narcolepsy type 2

ORPHA:83465Kr.
Unknown

Nasal ganglioglioma

ORPHA:141115Kr.

Nasal glial heterotopia

ORPHA:141112Kr.
Not applicable

Nasopharyngeal carcinoma

ORPHA:150Kr.
Multigenic/multifactorial, Not applicable

Navajo neurohepatopathy

ORPHA:255229Kr.
Autosomal recessive

Naxos disease

ORPHA:34217Kr.
Autosomal recessive

Necrobiosis lipoidica

ORPHA:542592Kr.

Necrobiotic xanthogranuloma

ORPHA:158011Kr.
Not applicable

Necrotizing enterocolitis

ORPHA:391673Kr.
Not applicable

Necrotizing soft tissue infection

ORPHA:440368Kr.
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 dermatomyositis

ORPHA:398117Kr.

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

Neonatal erythroderma-autoinflammation-inflammatory bowel disease syndrome

ORPHA:294023Kr.
Autosomal recessive

Neonatal hemochromatosis

ORPHA:446Kr.
Autosomal recessive

Neonatal ichthyosis-sclerosing cholangitis syndrome

ORPHA:59303Kr.
Autosomal recessive