BabelNet

bn:00870734n

Noun Concept

Categories: Syndromes, Syndromes with microcephaly, Genetics, HIV/AIDS

Aicardi–Goutières syndrome Aicardi-Goutieres syndrome Ags AGS1 Aicardi-Goutiere's

Aicardi–Goutières syndrome, which is completely distinct from the similarly named Aicardi syndrome, is a rare, usually early onset childhood, inflammatory disorder most typically affecting the brain and the skin. Wikipedia

Definitions

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Sources

A rare genetic disorder Wikipedia Disambiguation

Human disease Wikidata

IS A

DIFFERENT FROM

GENETIC ASSOCIATION

HEALTH SPECIALTY

Wikipedia

Aicardi–Goutières syndrome

Wikidata

Aicardi-Goutieres syndrome

Wikipedia Redirections

Aicardi-Goutiere's, Aicardi-Goutieres, Aicardi-Goutieres syndrome, Aicardi-Goutières syndrome, Aicardi–Goutieres syndrome, Cree encephalitis, pseudo-TORCH syndrome, Pseudotoxoplasmosis syndrome

Wikidata Alias

Ags, AGS1, AICARDI-GOUTIERES SYNDROME 1, Aicardi-Goutieres Syndrome 1, Autosomal Dominant, AICARDI-GOUTIERES SYNDROME 1; AGS1, Aicardi-Goutieres Syndrome type 1, Aicardi–Goutières syndrome, Cree encephalitis, Encephalopathy, Familial Infantile, With Intracranial Calcification and Chronic Cerebrospinal Fluid Lymphocytosis, Pseudotoxoplasmosis Syndrome