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
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Moynahan syndrome | Alopecia-epilepsy-intellectual disability syndrome, Moynahan type |
| fr | Syndrome de Moynahan | Syndrome d'alopécie-épilepsie-déficience intellectuelle |
| de | Moynahan-Syndrom | Alopezie-Epilepsie-Intelligenzminderung-Syndrom Typ Moynahan |
| es | Síndrome de Moynahan | Síndrome de alopecia-epilepsia-discapacidad intelectual, tipo Moynahan |
| it | Sindrome di Moynahan | Alopecia - epilessia - oligofrenia |
| nl | Syndroom van Moynahan | Alopecie - epilepsie - intellectuele achterstand-syndroom, Moynahan-type |
| pt | Síndrome Moynahan | Síndrome de alopecia-epilepsia-perturbação do desenvolvimento intelectual, tipo Moynahan |
| pl | Zespół Moynahana | Zespół łysienie-padaczka-oligofrenia, typu Moynahana |
| cs | Moynahanův syndrom | Syndrom zahrnující alopecii, epilepsii a oligofrenii, Moynahanův typ |
| uk | Синдром Мойнахена | Синдром алопеції-епілепсії-інтелектуальної недостатності, тип Мойнахана |
| zh | Moynahan综合征 | 脱发-癫痫-智力障碍综合征,Moynahan型 |
| tr | Moynahan sendromu | Alopesi-epilepsi-zihinsel yetersizlik sendromu, Moynahan tipi |
Definition in:
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 203600 | E | validated | |
| MONDO | 0008755 | E | validated | |
| MeSH | C537052 | E | validated | |
| UMLS | C0265328 | E | validated | |
| GARD | 606 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/2574
- This record as JSON: /data/d/2574.json