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Orphanet базасы

Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4,552Гендер
8,700Фенотиптер

Oculo-auriculo-vertebral spectrum

ORPHA:141132Мальф.
Not applicable

Oculo-palato-cerebral syndrome

ORPHA:2714Мальф.
Autosomal recessive

Oculoauricular syndrome, Schorderet type

ORPHA:157962Мальф.
Autosomal recessive

Oculoauriculofrontonasal syndrome

ORPHA:398156Мальф.
Unknown

Oculoauriculovertebral spectrum with radial defects

ORPHA:2549Мальф.

Oculocerebral hypopigmentation syndrome, Cross type

ORPHA:2719Мальф.

Oculocerebral hypopigmentation syndrome, Preus type

ORPHA:2720Мальф.

Oculocerebrocutaneous syndrome

ORPHA:1647Мальф.
Not applicable

Oculocerebrofacial syndrome, Kaufman type

ORPHA:2707Мальф.
Autosomal recessive

Oculocerebrorenal syndrome of Lowe

ORPHA:534Мальф.
X-linked recessive

Oculocutaneous albinism

ORPHA:55Клин. топ
Autosomal recessive

Oculocutaneous albinism type 1

ORPHA:352731Ауру
Autosomal recessive

Oculocutaneous albinism type 1A

ORPHA:79431Клин. под.
Autosomal recessive

Oculocutaneous albinism type 1B

ORPHA:79434Клин. под.
Autosomal recessive

Oculocutaneous albinism type 2

ORPHA:79432Ауру
Autosomal recessive

Oculocutaneous albinism type 3

ORPHA:79433Ауру
Autosomal recessive

Oculocutaneous albinism type 4

ORPHA:79435Ауру
Autosomal recessive

Oculocutaneous albinism type 5

ORPHA:370091Ауру
Autosomal recessive

Oculocutaneous albinism type 6

ORPHA:370097Ауру
Autosomal recessive

Oculocutaneous albinism type 7

ORPHA:352745Ауру
Autosomal recessive

Oculocutaneous albinism type 8

ORPHA:597733Ауру
Autosomal recessive

Oculodental syndrome, Rutherfurd type

ORPHA:2709Мальф.
Autosomal dominant

Oculodentodigital dysplasia

ORPHA:2710Мальф.
Autosomal dominant, Autosomal recessive

Oculoectodermal syndrome

ORPHA:3339Мальф.
Not applicable