MEDLIB
Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер

Open iniencephaly

ORPHA:268363Клин. под.
Multigenic/multifactorial, Not applicable

Open spinal dysraphism

ORPHA:268369Клин. топ
Multigenic/multifactorial, Not applicable

Open spinal dysraphism with a myelomeningocele

ORPHA:93969Морф.
Multigenic/multifactorial, Not applicable

Ophthalmological abnormalities-facial dysmorphism-intellectual disability syndrome

ORPHA:698090Мальф.
Autosomal dominant

Ophthalmomandibulomelic dysplasia

ORPHA:2741Мальф.

Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome

ORPHA:2743Мальф.

Opitz GBBB syndrome

ORPHA:2745Мальф.
X-linked recessive

Opsismodysplasia

ORPHA:2746Ауру
Autosomal recessive

Opsoclonus-myoclonus syndrome

ORPHA:1183Ауру
Not applicable

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

ORPHA:543470Ауру
Autosomal recessive

Optic atrophy-intellectual disability syndrome

ORPHA:401777Ауру
Autosomal dominant

Optic pathway glioma

ORPHA:2086Ауру
Not applicable

Oral submucous fibrosis

ORPHA:357154Ауру

Orbital leiomyoma

ORPHA:52994Ауру
Unknown

Orgasm-induced epilepsy

ORPHA:166421Ауру

Ornithine transcarbamylase deficiency

ORPHA:664Ауру
X-linked recessive

Orofacial clefting-cardiac anomalies-facial dysmorphism syndrome

ORPHA:660021Мальф.

Orofaciodigital syndrome type 1

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

Orofaciodigital syndrome type 11

ORPHA:141000Мальф.
Not applicable

Orofaciodigital syndrome type 14

ORPHA:434179Мальф.
Autosomal recessive

Orofaciodigital syndrome type 18

ORPHA:508501Мальф.
Autosomal recessive

Orofaciodigital syndrome type 2

ORPHA:2751Мальф.
Autosomal recessive

Orofaciodigital syndrome type 4

ORPHA:2753Мальф.
Autosomal recessive

Orofaciodigital syndrome type 5

ORPHA:2919Мальф.
Autosomal recessive