MEDLIB
Orphanet Database

Rare diseases

7,547 diseases with genetics, phenotypes, and epidemiology

7,547Diseases
4 552Genes
8 700Phenotypes

Open iniencephaly

ORPHA:268363Clin. sub.
Multigenic/multifactorial, Not applicable

Open spinal dysraphism

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

Open spinal dysraphism with a myelomeningocele

ORPHA:93969Morph.
Multigenic/multifactorial, Not applicable

Ophthalmological abnormalities-facial dysmorphism-intellectual disability syndrome

ORPHA:698090Malform.
Autosomal dominant

Ophthalmomandibulomelic dysplasia

ORPHA:2741Malform.

Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome

ORPHA:2743Malform.

Opitz GBBB syndrome

ORPHA:2745Malform.
X-linked recessive

Opsismodysplasia

ORPHA:2746Disease
Autosomal recessive

Opsoclonus-myoclonus syndrome

ORPHA:1183Disease
Not applicable

Optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome

ORPHA:543470Disease
Autosomal recessive

Optic atrophy-intellectual disability syndrome

ORPHA:401777Disease
Autosomal dominant

Optic pathway glioma

ORPHA:2086Disease
Not applicable

Oral submucous fibrosis

ORPHA:357154Disease

Orbital leiomyoma

ORPHA:52994Disease
Unknown

Orgasm-induced epilepsy

ORPHA:166421Disease

Ornithine transcarbamylase deficiency

ORPHA:664Disease
X-linked recessive

Orofacial clefting-cardiac anomalies-facial dysmorphism syndrome

ORPHA:660021Malform.

Orofaciodigital syndrome type 1

ORPHA:2750Malform.
Not applicable, X-linked dominant

Orofaciodigital syndrome type 11

ORPHA:141000Malform.
Not applicable

Orofaciodigital syndrome type 14

ORPHA:434179Malform.
Autosomal recessive

Orofaciodigital syndrome type 18

ORPHA:508501Malform.
Autosomal recessive

Orofaciodigital syndrome type 2

ORPHA:2751Malform.
Autosomal recessive

Orofaciodigital syndrome type 4

ORPHA:2753Malform.
Autosomal recessive

Orofaciodigital syndrome type 5

ORPHA:2919Malform.
Autosomal recessive