ORPHA:2739
Onycho-tricho-dysplasia-neutropenia syndrome
inactive · moved to ORPHA:33364Trichothiodystrophy
Synonyms: Itin syndrome · ONMR syndrome · Trichothiodystrophy type G
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Trichothiodystrophy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Onycho-tricho-dysplasia-neutropenia syndrome | Itin syndrome · ONMR syndrome · Trichothiodystrophy type G |
| fr | Syndrome d'onycho-tricho-dysplasie-neutropénie | Syndrome ONMR · Syndrome d'Itin · Trichothiodystrophie type G |
| de | Onycho-Tricho-Dysplasie - Neutropenie | Itin-Syndrom · ONMR-Syndrom · Trichothiodystrophie Typ G |
| es | Síndrome de onicotricodisplasia-neutropenia | Síndrome de Itin · Tricotiodistrofia tipo G |
| it | Onico-trico-displasia - neutropenia | Sindrome di Itin · Tricotiodistrofia, tipo G |
| nl | Onycho-tricho-dysplasie - neutropenie-syndroom | ONMR-syndroom · Syndroom van Itin · Trichothiodystrofie type G |
| pt | Síndrome de onico-trico-displasia-neutropenia | Síndrome Itin · Síndrome ONMR · Tricotiodistrofia tipo G |
| pl | Dysplazja paznokci i włosów z neutropenią | Trichotiodystrofia typu G · Zespół Itina · Zespół ONMR |
| cs | Syndrom zahrnující onychotrichodysplázii a neutropenii | ONMR syndrom · Trichothiodystrofie, typ G · Itinův syndrom |
| uk | Синдром оніхотриходисплазії-нейтропенії | Синдром Ітіна · Синдром ONMR · Трихотіодистрофія типу G |
| zh | 指甲-毛发-发育不良-中性粒细胞减少症综合征 | 毛发低硫营养不良,G型 |
| tr | Oniko-triko-displazi-nötropeni sendromu | Itin sendromu · ONMR sendromu · Trikotiyodistrofi tip G |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 258360 | E | validated | |
| UMLS | C1850316 | 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/2739
- This record as JSON: /data/d/2739.json