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База Orphanet

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4,552Гены
8,700Фенотипы

Non-syndromic pontocerebellar hypoplasia

ORPHA:98523Клин. гр.
Autosomal recessive

Non-syndromic posterior hypospadias

ORPHA:95706Морф.
Multigenic/multifactorial, X-linked recessive

Non-syndromic pouch colon

ORPHA:601013Морф.

Non-syndromic rectal atresia

ORPHA:601018Морф.

Non-syndromic rectal stenosis

ORPHA:601023Морф.

Non-syndromic rectourethral fistula

ORPHA:600961Морф.

Non-syndromic rectovaginal fistula

ORPHA:601028Морф.

Non-syndromic rectovesical fistula

ORPHA:600984Морф.

Non-syndromic sagittal craniosynostosis

ORPHA:35093Морф.
Autosomal dominant, Not applicable

Non-syndromic unicoronal and sagittal craniosynostosis

ORPHA:620186Морф.

Non-syndromic unicoronal craniosynostosis

ORPHA:620102Морф.

Non-syndromic unifrontosphenoidal craniosynostosis

ORPHA:620139Морф.

Non-syndromic unilambdoid craniosynostosis

ORPHA:620113Морф.

Non-syndromic unisquamosal craniosynostosis

ORPHA:620146Морф.

Non-syndromic vestibular fistula

ORPHA:600993Морф.

Noonan syndrome

ORPHA:648Порок
Autosomal dominant, Autosomal recessive

Noonan syndrome with multiple lentigines

ORPHA:500Порок
Autosomal dominant

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

ORPHA:363972Порок
Autosomal dominant

Noonan syndrome-like disorder with loose anagen hair

ORPHA:2701Порок
Autosomal dominant

Normosmic congenital hypogonadotropic hypogonadism

ORPHA:432Клин. подт.
Autosomal dominant, Autosomal recessive, Multigenic/multifactorial, X-linked recessive

Norrie disease

ORPHA:649Порок
X-linked recessive

North Carolina macular dystrophy

ORPHA:75327Заболевание
Autosomal dominant

Northern epilepsy

ORPHA:1947Клин. подт.
Autosomal recessive

Null pituitary adenoma

ORPHA:314790Гист. подт.
Not applicable