MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Iatrogenic botulism

ORPHA:254509Клин. подтип

Ichthyosis follicularis-alopecia-photophobia syndrome

ORPHA:2273Заболевание
Autosomal dominant, Not applicable, X-linked recessive

Ichthyosis hystrix of Curth-Macklin

ORPHA:79503Заболевание
Autosomal dominant, Not applicable

Ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome

ORPHA:2269Заболевание
Autosomal recessive

Ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome

ORPHA:2274Заболевание
Autosomal recessive, X-linked recessive

Ichthyosis-hypotrichosis syndrome

ORPHA:91132Заболевание
Autosomal recessive

Ichthyosis-intellectual disability-dwarfism-renal impairment syndrome

ORPHA:2278Мальформация

Ichthyosis-oral and digital anomalies syndrome

ORPHA:2272Мальформация
Autosomal recessive

Ichthyosis-prematurity syndrome

ORPHA:88621Заболевание
Autosomal recessive

Ichthyosis-short stature-brachydactyly-microspherophakia syndrome

ORPHA:363992Заболевание
Autosomal recessive

Idiopathic CD4 lymphocytopenia

ORPHA:228000Биоаномалия
Not applicable

Idiopathic achalasia

ORPHA:930Заболевание
Autosomal recessive, Not applicable

Idiopathic acute eosinophilic pneumonia

ORPHA:724Заболевание
Unknown

Idiopathic acute transverse myelitis

ORPHA:139423Клин. подтип
Not applicable

Idiopathic aplastic anemia

ORPHA:88Заболевание
Unknown

Idiopathic bronchiectasis

ORPHA:60033Заболевание
Not applicable

Idiopathic camptocormia

ORPHA:1320Морф. аномалия
Not applicable

Idiopathic catatonia

ORPHA:648919Заболевание

Idiopathic chronic eosinophilic pneumonia

ORPHA:2902Заболевание
Not applicable

Idiopathic chronic pancreatitis

ORPHA:700133Заболевание
Not applicable

Idiopathic congenital hypothyroidism

ORPHA:95717Заболевание

Idiopathic copper-associated cirrhosis

ORPHA:209919Заболевание
Unknown

Idiopathic dropped head syndrome

ORPHA:447881Clinical syndrome
Not applicable

Idiopathic ductopenia

ORPHA:480512Заболевание