MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

NLRP3-associated autoinflammatory disease

ORPHA:208650Kl. gruppe
Autosomal dominant, Not applicable

NMDA receptor encephalitis

ORPHA:217253Kr.
Not applicable

NOCARH syndrome

ORPHA:619363Kr.
Autosomal dominant

NPHP3-related Meckel-like syndrome

ORPHA:3032Malf.
Autosomal recessive

NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance

ORPHA:600663Malf.
Autosomal recessive

NTHL1-related polyposis

ORPHA:454840Kr.
Autosomal recessive

NUT midline carcinoma

ORPHA:443167Kr.
Not applicable

Naegeli-Franceschetti-Jadassohn syndrome

ORPHA:69087Kr.
Autosomal dominant

Nager syndrome

ORPHA:245Malf.
Autosomal dominant, Autosomal recessive, Not applicable

Nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome

ORPHA:423454Kr.
Autosomal recessive

Nail-patella syndrome

ORPHA:2614Malf.
Autosomal dominant

Nail-patella-like renal disease

ORPHA:2613Kr.
Autosomal dominant

Nance-Horan syndrome

ORPHA:627Malf.
X-linked dominant

Nanophthalmos

ORPHA:35612Malf.
Autosomal dominant, Autosomal recessive, Not applicable

Narcolepsy type 1

ORPHA:2073Kr.
Unknown

Narcolepsy type 2

ORPHA:83465Kr.
Unknown

Nasal encephalocele

ORPHA:141118Kl. subt.
Unknown

Nasal ganglioglioma

ORPHA:141115Kr.

Nasal glial heterotopia

ORPHA:141112Kr.
Not applicable

Nasolacrimal duct cyst

ORPHA:141083Morph.
Not applicable

Nasopalpebral lipoma-coloboma syndrome

ORPHA:2399Malf.
Autosomal dominant

Nasopharyngeal carcinoma

ORPHA:150Kr.
Multigenic/multifactorial, Not applicable

Nasu-Hakola disease

ORPHA:2770Malf.
Autosomal recessive

Nathalie syndrome

ORPHA:2663Malf.