MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes
727 diseases matched (Clin. sub.) Reset

Multisystem Langerhans cell histiocytosis

ORPHA:687741Clin. sub.
Not applicable

Myelodysplastic neoplasm with increased blasts type 1

ORPHA:100019Clin. sub.
Not applicable

Myelodysplastic neoplasm with increased blasts type 2

ORPHA:100020Clin. sub.
Not applicable

Nasal encephalocele

ORPHA:141118Clin. sub.
Unknown

Necrotizing cellulitis

ORPHA:699678Clin. sub.
Not applicable

Necrotizing fasciitis

ORPHA:699697Clin. sub.
Not applicable

Necrotizing myositis

ORPHA:699702Clin. sub.
Not applicable

Neonatal glycine encephalopathy

ORPHA:289857Clin. sub.
Autosomal recessive

Neurogenic thoracic outlet syndrome

ORPHA:100073Clin. sub.
Not applicable

Niemann-Pick disease type C, adult neurologic onset

ORPHA:216986Clin. sub.
Autosomal recessive

Niemann-Pick disease type C, juvenile neurologic onset

ORPHA:216981Clin. sub.
Autosomal recessive

Niemann-Pick disease type C, late infantile neurologic onset

ORPHA:216978Clin. sub.
Autosomal recessive

Niemann-Pick disease type C, severe early infantile neurologic onset

ORPHA:216975Clin. sub.
Autosomal recessive

Niemann-Pick disease type C, severe perinatal form

ORPHA:216972Clin. sub.
Autosomal recessive

Nodular urticaria pigmentosa

ORPHA:158772Clin. sub.
Autosomal dominant, Unknown

Non-classic congenital lipoid adrenal hyperplasia due to STAR deficency

ORPHA:325529Clin. sub.
Autosomal recessive

Non-fibrotic hypersensitivity pneumonitis

ORPHA:686462Clin. sub.
Not applicable

Non-hereditary retinoblastoma

ORPHA:357034Clin. sub.
Not applicable

Non-immune hydrops fetalis

ORPHA:363999Clin. sub.
Not applicable

Normosmic congenital hypogonadotropic hypogonadism

ORPHA:432Clin. sub.
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive

Northern epilepsy

ORPHA:1947Clin. sub.
Autosomal recessive

Null syndrome

ORPHA:280234Clin. sub.
X-linked recessive

Occipital encephalocele

ORPHA:268823Clin. sub.
Autosomal dominant

Ocular cystinosis

ORPHA:411641Clin. sub.
Autosomal recessive