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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

NEK9-related lethal skeletal dysplasia

ORPHA:464366Мальф.
Autosomal recessive

NKAP-related intellectual disability-facial dysmorphism-marfanoid habitus-scoliosis syndrome

ORPHA:700325Мальф.
X-linked recessive

NPHP3-related Meckel-like syndrome

ORPHA:3032Мальф.
Autosomal recessive

NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance

ORPHA:600663Мальф.
Autosomal recessive

Nager syndrome

ORPHA:245Мальф.
Autosomal dominant, Autosomal recessive, Not applicable

Nail-patella syndrome

ORPHA:2614Мальф.
Autosomal dominant

Nance-Horan syndrome

ORPHA:627Мальф.
X-linked dominant

Nanophthalmos

ORPHA:35612Мальф.
Autosomal dominant, Autosomal recessive, Not applicable

Nasopalpebral lipoma-coloboma syndrome

ORPHA:2399Мальф.
Autosomal dominant

Nasu-Hakola disease

ORPHA:2770Мальф.
Autosomal recessive

Nathalie syndrome

ORPHA:2663Мальф.

Native American myopathy

ORPHA:168572Мальф.
Autosomal recessive

Nephropathy-deafness-hyperparathyroidism syndrome

ORPHA:2668Мальф.
Autosomal recessive

Nephrosis-deafness-urinary tract-digital malformations syndrome

ORPHA:2669Мальф.
Unknown

Nestor-Guillermo progeria syndrome

ORPHA:280576Мальф.
Autosomal recessive

Neu-Laxova syndrome

ORPHA:2671Мальф.
Autosomal recessive

Neuhauser-Eichner-Opitz syndrome

ORPHA:2672Мальф.
Autosomal dominant

Neurodevelopmental delay-brain malformations-skeletal defects-intellectual disability syndrome

ORPHA:662207Мальф.
Autosomal dominant

Neurodevelopmental delay-congenital heart defects-intellectual disability syndrome

ORPHA:662234Мальф.
Autosomal dominant

Neurodevelopmental delay-intellectual disability-skeletal defects syndrome

ORPHA:662198Мальф.
X-linked dominant

Neurodevelopmental delay-seizures-ophthalmic anomalies-osteopenia-cerebellar atrophy syndrome

ORPHA:529665Мальф.
Autosomal recessive

Neurodevelopmental disorder-brain malformation-facial dysmorphism-brachydactyly syndrome

ORPHA:662189Мальф.
Autosomal dominant

Neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-skeletal anomalies syndrome

ORPHA:453499Мальф.
Autosomal dominant, Not applicable

Neurodevelopmental disorder-slit-like lateral ventricles-intellectual disability syndrome

ORPHA:664430Мальф.
Autosomal recessive