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Сирек аурулар

7,547 ауру гендер, фенотиптер және эпидемиологиямен

7,547Аурулар
4 552Гендер
8 700Фенотиптер
Табылды 1,772 заболеваний (Мальф.) Қалпына келтіру

Weismann-Netter syndrome

ORPHA:3344Мальф.

Weiss-Kruszka Syndrome

ORPHA:502430Мальф.
Autosomal dominant

White forelock with malformations

ORPHA:2475Мальф.

White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome

ORPHA:3207Мальф.

Wieacker-Wolff syndrome

ORPHA:3454Мальф.
Not applicable, X-linked recessive

Wiedemann-Rautenstrauch syndrome

ORPHA:3455Мальф.
Autosomal recessive

Wiedemann-Steiner syndrome

ORPHA:319182Мальф.
Autosomal dominant

Wildervanck syndrome

ORPHA:3456Мальф.

Williams syndrome

ORPHA:904Мальф.
Autosomal dominant

Wilson-Turner syndrome

ORPHA:3459Мальф.
X-linked dominant, X-linked recessive

Witteveen-Kolk syndrome

ORPHA:500163Мальф.
Autosomal dominant

Wolf-Hirschhorn syndrome

ORPHA:280Мальф.
Multigenic/multifactorial, Not applicable

Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia

ORPHA:166277Мальф.
Unknown

Wormian bones-micrognathia-abnormal dentition-progeroid syndrome

ORPHA:659873Мальф.
Autosomal dominant

X small rings syndrome

ORPHA:96201Мальф.

X-linked alpha-thalassemia-intellectual disability syndrome

ORPHA:847Мальф.
X-linked recessive

X-linked cleft palate and ankyloglossia

ORPHA:324601Мальф.
X-linked dominant, X-linked recessive

X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome

ORPHA:431140Мальф.
X-linked recessive

X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome

ORPHA:500188Мальф.
X-linked recessive

X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability

ORPHA:480880Мальф.
X-linked dominant

X-linked intellectual disability, Abidi type

ORPHA:85273Мальф.
X-linked recessive

X-linked intellectual disability, Armfield type

ORPHA:85276Мальф.
X-linked recessive

X-linked intellectual disability, Cabezas type

ORPHA:85293Мальф.
X-linked recessive

X-linked intellectual disability, Cantagrel type

ORPHA:85277Мальф.
X-linked recessive