MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Native American myopathy

ORPHA:168572Мальформация
Autosomal recessive

Navajo neurohepatopathy

ORPHA:255229Заболевание
Autosomal recessive

Naxos disease

ORPHA:34217Заболевание
Autosomal recessive

Necrobiosis lipoidica

ORPHA:542592Заболевание

Necrobiotic xanthogranuloma

ORPHA:158011Заболевание
Not applicable

Necrotizing cellulitis

ORPHA:699678Клин. подтип
Not applicable

Necrotizing enterocolitis

ORPHA:391673Заболевание
Not applicable

Necrotizing fasciitis

ORPHA:699697Клин. подтип
Not applicable

Necrotizing myositis

ORPHA:699702Клин. подтип
Not applicable

Necrotizing soft tissue infection

ORPHA:440368Заболевание
Not applicable

Nelson syndrome

ORPHA:199244Clinical syndrome

Nemaline myopathy

ORPHA:607Клин. группа
Autosomal dominant, Autosomal recessive, Not applicable

Neonatal Marfan syndrome

ORPHA:284979Заболевание
Autosomal dominant

Neonatal acute respiratory distress syndrome

ORPHA:217563Заболевание
Autosomal recessive

Neonatal adrenoleukodystrophy

ORPHA:44Заболевание
Autosomal recessive

Neonatal alloimmune neutropenia

ORPHA:464370Заболевание

Neonatal antiphospholipid syndrome

ORPHA:398097Заболевание

Neonatal autoimmune hemolytic anemia

ORPHA:398109Заболевание

Neonatal compartment syndrome

ORPHA:641829Clinical syndrome

Neonatal dermatomyositis

ORPHA:398117Заболевание

Neonatal diabetes mellitus

ORPHA:224Категория
Autosomal dominant, Autosomal recessive, Not applicable

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

ORPHA:79118Заболевание
Autosomal recessive

Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

ORPHA:457185Заболевание
Autosomal recessive

Neonatal epileptic encephalopathy due to glutaminase deficiency

ORPHA:557064Заболевание
Autosomal recessive