MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

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

Open iniencephaly

ORPHA:268363Kl. subt.
Multigenic/multifactorial, Not applicable

Open spinal dysraphism

ORPHA:268369Kl. gruppe
Multigenic/multifactorial, Not applicable

Open spinal dysraphism with a myelomeningocele

ORPHA:93969Morph.
Multigenic/multifactorial, Not applicable

Ophthalmological abnormalities-facial dysmorphism-intellectual disability syndrome

ORPHA:698090Malf.
Autosomal dominant

Ophthalmomandibulomelic dysplasia

ORPHA:2741Malf.

Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome

ORPHA:2743Malf.

Opitz GBBB syndrome

ORPHA:2745Malf.
X-linked recessive

Opsismodysplasia

ORPHA:2746Kr.
Autosomal recessive

Opsoclonus-myoclonus syndrome

ORPHA:1183Kr.
Not applicable

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

ORPHA:543470Kr.
Autosomal recessive

Optic atrophy-intellectual disability syndrome

ORPHA:401777Kr.
Autosomal dominant

Optic pathway glioma

ORPHA:2086Kr.
Not applicable

Oral submucous fibrosis

ORPHA:357154Kr.

Orbital leiomyoma

ORPHA:52994Kr.
Unknown

Orgasm-induced epilepsy

ORPHA:166421Kr.

Ornithine transcarbamylase deficiency

ORPHA:664Kr.
X-linked recessive

Orofacial clefting-cardiac anomalies-facial dysmorphism syndrome

ORPHA:660021Malf.

Orofaciodigital syndrome type 1

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

Orofaciodigital syndrome type 11

ORPHA:141000Malf.
Not applicable

Orofaciodigital syndrome type 14

ORPHA:434179Malf.
Autosomal recessive

Orofaciodigital syndrome type 18

ORPHA:508501Malf.
Autosomal recessive

Orofaciodigital syndrome type 2

ORPHA:2751Malf.
Autosomal recessive

Orofaciodigital syndrome type 4

ORPHA:2753Malf.
Autosomal recessive

Orofaciodigital syndrome type 5

ORPHA:2919Malf.
Autosomal recessive