ORPHA:2861
OBSOLETE: Short stature-microcephaly-heart defect syndrome
inactive · referred to ORPHA:102369Rare syndromic intellectual disability
Synonyms: OBSOLETE: D'Ercole syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Rare syndromic intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Short stature-microcephaly-heart defect syndrome | OBSOLETE: D'Ercole syndrome |
| fr | OBSOLETE : Syndrome de petite taille-microcéphalie-cardiopathie | OBSOLETE : Syndrome de D'Ercole |
| de | OBSOLET: Kleinwuchs-Mikrozephalie-Herzfehler-Syndrom | OBSOLET: D'Ercole-Syndrom |
| es | OBSOLETO: Síndrome de talla baja-microcefalia-defecto cardíaco | OBSOLETO: Síndrome de D'Ercole |
| it | OBSOLETO: Sindeome bassa statura-microcefalia-cardiopatia | OBSOLETO: Sindrome di D'Ercole |
| nl | OBSOLEET: Kleine gestalte - microcefalie - hartdefect-syndroom | OBSOLEET: Syndroom van D'Ercole |
| pt | OBSOLETO: Síndrome de baixa estatura-microcefalia-defeito cardíaco | OBSOLETO: Síndrome D'Ercole |
| pl | NIEAKTUALNE: Niski wzrost - maloglowie - wada serca | NIEAKTUALNE: Zespół D'Ercole |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující nízký vzrůst, mikrocefalii a srdeční vady | = en |
| uk | ЗАСТАРІЛО: Синдром низькорослості-мікроцефалії-серцевої вади | ЗАСТАРІЛО: Синдром ДЕрколя |
| zh | 弃用:身材矮小-小头畸形-心脏缺陷综合征 | D'Ercole综合征 |
| tr | Eski adı: Kısa boy-mikrosefali-kalp defekti sendromu | D'Ercole sendromu |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/2861
- This record as JSON: /data/d/2861.json