MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

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

Müllerian aplasia

ORPHA:73217Clin. grp.
Autosomal dominant

NLRP3-associated autoinflammatory disease

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

Nemaline myopathy

ORPHA:607Clin. grp.
Autosomal dominant, Autosomal recessive, Not applicable

Neuroacanthocytosis

ORPHA:263440Clin. grp.

Neurodegeneration with brain iron accumulation

ORPHA:385Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked dominant

Neuronal ceroid lipofuscinosis

ORPHA:216Clin. grp.
Autosomal dominant, Autosomal recessive

Neutral lipid storage disease

ORPHA:165Clin. grp.
Autosomal recessive

Non-histaminic angioedema

ORPHA:658Clin. grp.
Autosomal dominant, Not applicable

Non-rhizomelic chondrodysplasia punctata

ORPHA:176Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked dominant, X-linked recessive

Non-syndromic anorectal malformation

ORPHA:557Clin. grp.

Non-syndromic craniosynostosis

ORPHA:139390Clin. grp.

Non-syndromic hemimelia

ORPHA:2130Clin. grp.
Not applicable

Non-syndromic pontocerebellar hypoplasia

ORPHA:98523Clin. grp.
Autosomal recessive

Oblique facial cleft

ORPHA:141253Clin. grp.

Oculocutaneous albinism

ORPHA:55Clin. grp.
Autosomal recessive

Oligoastrocytic tumor

ORPHA:251651Clin. grp.

Oligodendroglial tumor

ORPHA:46484Clin. grp.
Multigenic/multifactorial, Not applicable

Open spinal dysraphism

ORPHA:268369Clin. grp.
Multigenic/multifactorial, Not applicable

Oromandibular-limb hypogenesis syndrome

ORPHA:2749Clin. grp.

Osteopetrosis and related disorders

ORPHA:2781Clin. grp.
Autosomal dominant, Autosomal recessive, X-linked recessive

Paramedian facial cleft

ORPHA:155867Clin. grp.

Paroxysmal dyskinesia

ORPHA:1431Clin. grp.
Autosomal dominant, Not applicable

Peeling skin syndrome

ORPHA:817Clin. grp.
Autosomal recessive

Peroxisome biogenesis disorder

ORPHA:79189Clin. grp.
Autosomal recessive