ORPHA:3065

X-linked intellectual disability-monoamine oxidase A metabolism anomaly syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Monoamine oxidase A deficiency

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	X-linked intellectual disability-monoamine oxidase A metabolism anomaly syndrome
fr	Syndrome de déficience intellectuelle liée à l'X-anomalie du métabolisme de la monoamine oxydase A
de	X-chromosomale Intelligenzminderung mit Monoaminooxidase-A-Stoffwechselstörung
es	Síndrome de discapacidad intelectual-anomalía del metabolismo de la monoamino oxidasa A ligado al cromosoma X
it	Sindrome disabilità intellettiva legata all'X-anomalia del metabolismo della monoaminossidasi A
nl	X-gebonden intellectuele achterstand - monoamine-oxidase A-stofwisselingsdefect-syndroom
pt	Síndrome de perturbação do desenvolvimento intelectual ligeira-anomalias do metabolismo da monoamino-oxidase A ligada ao X
pl	Niepełnosprawność intelektualna sprzężona z chromosomem X - nieprawidłowy metabolizm oksydazy monoaminowej A
cs	Syndrom zahrnující X-vázané mentální postižení a anomálii metabolismu monoaminoxidázy A
uk	Х-зчеплена розумова відсталість та синдром аномалії метаболізму моноаміноксидази А
zh	X连锁智力障碍-单胺氧化酶A代谢异常综合征
tr	X'e bağlı zihinsel yetersizlik-monoamin oksidaz A metabolizma anomalisi sendromu

qualifier = Orphanet mapping relation

No cross-references in this release.

Not placed in any Orphanet classification in this release.

No children.

0 direct

Orphanet records no gene directly on this code.

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.