ORPHA:137658
Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome
inactive · moved to ORPHA:3255Filippi syndrome
Synonyms: Woods-Crouchman-Huson syndrome
- 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 Filippi syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome | Woods-Crouchman-Huson syndrome |
| fr | Syndrome de microcéphalie-déficience intellectuelle-anomalies neurologiques et des phalanges | Syndrome de Woods-Crouchman-Huson |
| de | Mikrozephalie-Intelligenzminderung-phalangeale und neurologische Anomalien-Syndrom | Woods-Crouchman-Huson-Syndrom |
| es | Síndrome de microcefalia-discapacidad intelectual-anomalías falángicas y neurológicas | Síndrome de Woods-Crouchman-Huson |
| it | Sindrome microcefalia-deficit cognitivo-anomalie neurologiche e falangee | Sindrome di Woods-Crouchman-Huson |
| nl | Microcefalie - intellectuele achterstand - falangeale en neurologische anomalieën-syndroom | Syndroom van Woods-Crouchman-Huson |
| pt | Síndrome de microcefalia-perturbação do desenvolvimento intelectual-anomalias das falanges e neurológicas | Síndrome Woods-Crouchman-Huson |
| pl | Małogłowie - niepełnosprawność intelektualna - wady paliczków i zaburzenia neurologiczne | Zespół Woodsa, Crouchmana i Husona |
| cs | Syndrom zahrnující mikrocefalii, mentální retardaci, anomálie falangů a neurologické anomálie | Woodsův-Crouchmanův-Husonův syndrom · Woods-Crouchman-Husonův syndrom |
| uk | Синдром мікроцефалії-інтелектуальної недостатності-фалангових та неврологічних аномалій | Синдром Вудса-Краучмана-Хьюсона |
| zh | 小头畸形-智力障碍-指和神经异常综合征 | Woods-Crouchman-Huson综合征 |
| tr | Mikrosefali-zihinsel yetersizlik-falanjiyal ve nörolojik anomaliler sendromu | Woods-Crouchman-Huson sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 615236 | 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/137658
- This record as JSON: /data/d/137658.json