MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов
Найдено 1,772 заболеваний (Мальформация)Сбросить

NEK9-related lethal skeletal dysplasia

ORPHA:464366Мальформация
Autosomal recessive

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

ORPHA:700325Мальформация
X-linked recessive

NPHP3-related Meckel-like syndrome

ORPHA:3032Мальформация
Autosomal recessive

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

ORPHA:600663Мальформация
Autosomal recessive

Nager syndrome

ORPHA:245Мальформация
Autosomal dominant, Autosomal recessive, Not applicable

Nail-patella syndrome

ORPHA:2614Мальформация
Autosomal dominant

Nance-Horan syndrome

ORPHA:627Мальформация
X-linked dominant

Nanophthalmos

ORPHA:35612Мальформация
Autosomal dominant, Autosomal recessive, Not applicable

Nasopalpebral lipoma-coloboma syndrome

ORPHA:2399Мальформация
Autosomal dominant

Nasu-Hakola disease

ORPHA:2770Мальформация
Autosomal recessive

Nathalie syndrome

ORPHA:2663Мальформация

Native American myopathy

ORPHA:168572Мальформация
Autosomal recessive

Nephropathy-deafness-hyperparathyroidism syndrome

ORPHA:2668Мальформация
Autosomal recessive

Nephrosis-deafness-urinary tract-digital malformations syndrome

ORPHA:2669Мальформация
Unknown

Nestor-Guillermo progeria syndrome

ORPHA:280576Мальформация
Autosomal recessive

Neu-Laxova syndrome

ORPHA:2671Мальформация
Autosomal recessive

Neuhauser-Eichner-Opitz syndrome

ORPHA:2672Мальформация
Autosomal dominant

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

ORPHA:662207Мальформация
Autosomal dominant

Neurodevelopmental delay-congenital heart defects-intellectual disability syndrome

ORPHA:662234Мальформация
Autosomal dominant

Neurodevelopmental delay-intellectual disability-skeletal defects syndrome

ORPHA:662198Мальформация
X-linked dominant

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

ORPHA:529665Мальформация
Autosomal recessive

Neurodevelopmental disorder-brain malformation-facial dysmorphism-brachydactyly syndrome

ORPHA:662189Мальформация
Autosomal dominant

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

ORPHA:453499Мальформация
Autosomal dominant, Not applicable

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

ORPHA:664430Мальформация
Autosomal recessive