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Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Заболевания
4 552Гены
8 700Фенотипы

Native American myopathy

ORPHA:168572Malform.
Autosomal recessive

Navajo neurohepatopathy

ORPHA:255229Disease
Autosomal recessive

Naxos disease

ORPHA:34217Disease
Autosomal recessive

Necrobiosis lipoidica

ORPHA:542592Disease

Necrobiotic xanthogranuloma

ORPHA:158011Disease
Not applicable

Necrotizing cellulitis

ORPHA:699678Clin. sub.
Not applicable

Necrotizing enterocolitis

ORPHA:391673Disease
Not applicable

Necrotizing fasciitis

ORPHA:699697Clin. sub.
Not applicable

Necrotizing myositis

ORPHA:699702Clin. sub.
Not applicable

Necrotizing soft tissue infection

ORPHA:440368Disease
Not applicable

Nelson syndrome

ORPHA:199244Clinical syndrome

Nemaline myopathy

ORPHA:607Clin. grp.
Autosomal dominant, Autosomal recessive, Not applicable

Neonatal Marfan syndrome

ORPHA:284979Disease
Autosomal dominant

Neonatal acute respiratory distress syndrome

ORPHA:217563Disease
Autosomal recessive

Neonatal adrenoleukodystrophy

ORPHA:44Disease
Autosomal recessive

Neonatal alloimmune neutropenia

ORPHA:464370Disease

Neonatal antiphospholipid syndrome

ORPHA:398097Disease

Neonatal autoimmune hemolytic anemia

ORPHA:398109Disease

Neonatal compartment syndrome

ORPHA:641829Clinical syndrome

Neonatal dermatomyositis

ORPHA:398117Disease

Neonatal diabetes mellitus

ORPHA:224Cat.
Autosomal dominant, Autosomal recessive, Not applicable

Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome

ORPHA:79118Disease
Autosomal recessive

Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

ORPHA:457185Disease
Autosomal recessive

Neonatal epileptic encephalopathy due to glutaminase deficiency

ORPHA:557064Disease
Autosomal recessive