ORPHA:3084

Mirhosseini-Holmes-Walton syndrome

Synonyms: Pigmentary retinopathy-intellectual disability syndrome

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Cohen syndrome

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Mirhosseini-Holmes-Walton syndrome	Pigmentary retinopathy-intellectual disability syndrome
fr	Syndrome de Mirhosseini-Holmes-Walton	Syndrome de rétinite pigmentaire-déficience intellectuelle
de	Mirhosseini-Holmes-Walton-Syndrom	Pigmentretinopathie-Intelligenzminderung-Syndrom
es	Síndrome de Morhosseini-Holmes-Walton	Síndrome de retinopatía pigmentaria-discapacidad intelectual
it	Sindrome di Morhosseini-Holmes-Walton	Sindrome retinite pigmentosa-disabilità intellettiva
nl	Syndroom van Mirhosseini-Holmes-Walton	Pigmentretinopathie - intellectuele achterstand-syndroom
pt	Síndrome Morhosseini-Holmes-Walton	Síndrome de retinopatia pigmentosa-perturbação do desenvolvimento intelectual
pl	Zespół Mirhosseini, Holmesa i Waltona	Retinopatia barwnikowa - niepełnosprawność intelektualna
cs	Mirhosseiniho-Holmesův-Waltonův syndrom	Syndrom zahrnující pigmentovou retinopatii a mentální retardaci · Mirhosseini-Holmes-Waltonův syndrom
uk	Синдром Мірхосейні-Холмса-Уолтона	Синдром пігментної ретинопатії - інтелектуальної недостатності
zh	Mirhosseini-Holmes-Walton综合征	色素性视网膜病-智力障碍综合征
tr	Mirhosseini-Holmes-Walton sendromu	Pigmenter retinopati-zihinsel yetersizlik sendromu

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
OMIM	268050	E		validated
UMLS	C0796072	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

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.