MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

NLRP3-associated autoinflammatory disease

ORPHA:208650Clin. grp.
Autosomal dominant, Not applicable

NMDA receptor encephalitis

ORPHA:217253Disease
Not applicable

NOCARH syndrome

ORPHA:619363Disease
Autosomal dominant

NPHP3-related Meckel-like syndrome

ORPHA:3032Malform.
Autosomal recessive

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

ORPHA:600663Malform.
Autosomal recessive

NTHL1-related polyposis

ORPHA:454840Disease
Autosomal recessive

NUT midline carcinoma

ORPHA:443167Disease
Not applicable

Naegeli-Franceschetti-Jadassohn syndrome

ORPHA:69087Disease
Autosomal dominant

Nager syndrome

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

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

ORPHA:423454Disease
Autosomal recessive

Nail-patella syndrome

ORPHA:2614Malform.
Autosomal dominant

Nail-patella-like renal disease

ORPHA:2613Disease
Autosomal dominant

Nance-Horan syndrome

ORPHA:627Malform.
X-linked dominant

Nanophthalmos

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

Narcolepsy type 1

ORPHA:2073Disease
Unknown

Narcolepsy type 2

ORPHA:83465Disease
Unknown

Nasal encephalocele

ORPHA:141118Clin. sub.
Unknown

Nasal ganglioglioma

ORPHA:141115Disease

Nasal glial heterotopia

ORPHA:141112Disease
Not applicable

Nasolacrimal duct cyst

ORPHA:141083Morph.
Not applicable

Nasopalpebral lipoma-coloboma syndrome

ORPHA:2399Malform.
Autosomal dominant

Nasopharyngeal carcinoma

ORPHA:150Disease
Multigenic/multifactorial, Not applicable

Nasu-Hakola disease

ORPHA:2770Malform.
Autosomal recessive

Nathalie syndrome

ORPHA:2663Malform.