raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:2574

Moynahan syndrome

inactive · moved to ORPHA:2850Alopecia-intellectual disability syndrome

Synonyms: Alopecia-epilepsy-intellectual disability syndrome, Moynahan type

Type
Malformation syndrome
Group
Disorder
Status
inactive
Flag
Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Alopecia-intellectual disability syndrome

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMoynahan syndromeAlopecia-epilepsy-intellectual disability syndrome, Moynahan type
frSyndrome de MoynahanSyndrome d'alopécie-épilepsie-déficience intellectuelle
deMoynahan-SyndromAlopezie-Epilepsie-Intelligenzminderung-Syndrom Typ Moynahan
esSíndrome de MoynahanSíndrome de alopecia-epilepsia-discapacidad intelectual, tipo Moynahan
itSindrome di MoynahanAlopecia - epilessia - oligofrenia
nlSyndroom van MoynahanAlopecie - epilepsie - intellectuele achterstand-syndroom, Moynahan-type
ptSíndrome MoynahanSíndrome de alopecia-epilepsia-perturbação do desenvolvimento intelectual, tipo Moynahan
plZespół MoynahanaZespół łysienie-padaczka-oligofrenia, typu Moynahana
csMoynahanův syndromSyndrom zahrnující alopecii, epilepsii a oligofrenii, Moynahanův typ
ukСиндром МойнахенаСиндром алопеції-епілепсії-інтелектуальної недостатності, тип Мойнахана
zhMoynahan综合征脱发-癫痫-智力障碍综合征,Moynahan型
trMoynahan sendromuAlopesi-epilepsi-zihinsel yetersizlik sendromu, Moynahan tipi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
OMIM203600Evalidated
MONDO0008755Evalidated
MeSHC537052Evalidated
UMLSC0265328Evalidated
GARD606Evalidated

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

3

Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

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

7

Sources for this card