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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

Mucocutaneous venous malformations

ORPHA:2451Мальф.
Autosomal dominant

Mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders

ORPHA:505248Мальф.
Autosomal recessive

Muenke syndrome

ORPHA:53271Мальф.
Autosomal dominant

Mulibrey nanism

ORPHA:2576Мальф.
Autosomal recessive

Multicentric carpo-tarsal osteolysis with or without nephropathy

ORPHA:2774Мальф.
Autosomal dominant

Multinodular goiter-cystic kidney-polydactyly syndrome

ORPHA:2091Мальф.
Autosomal dominant

Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome

ORPHA:500135Мальф.
Autosomal recessive

Multiple congenital anomalies-hypotonia-seizures syndrome

ORPHA:280633Мальф.
Autosomal recessive

Multiple congenital anomalies-hypotonia-seizures syndrome type 2

ORPHA:300496Мальф.
X-linked recessive

Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome

ORPHA:659904Мальф.
Autosomal dominant

Multiple pterygium-malignant hyperthermia syndrome

ORPHA:2215Мальф.
Autosomal recessive

Multiple synostoses syndrome

ORPHA:3237Мальф.
Autosomal dominant

Muscle-eye-brain disease

ORPHA:588Мальф.
Autosomal recessive

Muscular hypertrophy-hepatomegaly-polyhydramnios syndrome

ORPHA:324416Мальф.
Autosomal dominant

Myalgia-eosinophilia syndrome associated with tryptophan

ORPHA:2582Мальф.
Not applicable

Mycophenolate mofetil embryopathy

ORPHA:268249Мальф.
Not applicable

Myhre syndrome

ORPHA:2588Мальф.
Autosomal dominant

Myoclonic epilepsy in non-progressive encephalopathies

ORPHA:86913Мальф.

Myoclonus-cerebellar ataxia-deafness syndrome

ORPHA:2589Мальф.
Autosomal dominant

Müllerian aplasia and hyperandrogenism

ORPHA:247768Мальф.
Autosomal dominant, Not applicable

Müllerian derivatives-lymphangiectasia-polydactyly syndrome

ORPHA:1655Мальф.
Unknown

Müllerian duct anomalies-limb anomalies syndrome

ORPHA:2491Мальф.

N syndrome

ORPHA:2608Мальф.
X-linked recessive

NDE1-related microhydranencephaly

ORPHA:443162Мальф.
Autosomal recessive