Brunner Syndrome
amino acid metabolic disorder characterized by recessive X-linked inhetiance, impaired monoamine metabolism, impulsive aggressiveness and mild mental retardation that has material basis in mutation in the MAOA gene on chromosome location Xp11
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Brunner Syndrome
Summary
Brunner Syndrome is a rare disease[1]. It draws 122 Wikipedia views per month (rare_disease category, ranking #145 of 627).[2]
Key Facts
- Brunner Syndrome's instance of is recorded as rare disease[3].
- Brunner Syndrome's instance of is recorded as class of disease[4].
- Brunner Syndrome's subclass of is recorded as amino acid metabolic disorder[5].
- Brunner Syndrome's subclass of is recorded as syndromic neurometabolic disease with X-linked intellectual disability[6].
- Brunner Syndrome's subclass of is recorded as inborn disorder of neurotransmitter metabolism and transport[7].
- Brunner Syndrome's subclass of is recorded as X-linked recessive disease[8].
- Brunner Syndrome's MeSH descriptor ID is recorded as C563156[9].
- Brunner Syndrome's OMIM ID is recorded as 300615[10].
- Brunner Syndrome's DiseasesDB is recorded as 32391[11].
- Brunner Syndrome's KEGG ID is recorded as H00548[12].
- Brunner Syndrome's Disease Ontology ID is recorded as DOID:0060693[13].
- Brunner Syndrome's Orphanet ID is recorded as 3057[14].
- Brunner Syndrome's genetic association is recorded as MAOA[15].
- Brunner Syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060693[16].
- Brunner Syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060693[17].
- Brunner Syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3057[18].
- Brunner Syndrome's UMLS CUI is recorded as C0796275[19].
- Brunner Syndrome's ICD-10-CM is recorded as E70.8[20].
- Brunner Syndrome's GARD rare disease ID is recorded as 3531[21].
- Brunner Syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[22].
- Brunner Syndrome's Mondo ID is recorded as MONDO_0010379[23].
- Brunner Syndrome's Microsoft Academic ID is recorded as 2778694968[24].
- Brunner Syndrome's UniProt disease ID is recorded as DI-00206[25].
Why It Matters
Brunner Syndrome draws 122 Wikipedia views per month (rare_disease category, ranking #145 of 627).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[26] It is known by 7 alternative names across languages and contexts.[27]