ORPHA:101091
Hyper-IgM syndrome type 4
Synonyms: HIGM4
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Hyper-IgM syndrome without susceptibility to opportunistic infections
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hyper-IgM syndrome type 4 | HIGM4 |
| fr | Syndrome hyper-IgM type 4 | = en |
| de | Hyper-IgM-Syndrom Typ 4 | = en |
| es | Síndrome hiper-IgM tipo 4 | = en |
| it | Sindrome iper-IgM, tipo 4 | = en |
| nl | Hyper-IgM-syndroom type 4 | = en |
| pt | Síndrome hiper-IgM tipo 4 | |
| pl | Zespół hiper-IgM typu 4 | = en |
| cs | Hyper-IgM syndrom, typ 4 | HIGM4 · Syndrom hyperimunoglobulinemie IgM, typ 4 |
| uk | Синдром гіпер-IgM, тип 4 | = en |
| zh | 高IgM综合征4型 | = en |
| tr | Hiper-IgM sendromu tip 4 | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 608184 | E | validated | |
| ICD-10 | D80.5 | NTBT | attributed | validated |
| ICD-11 | 4A01.1Y | NTBT | attributed | validated |
| MONDO | 0011985 | E | validated | |
| MeSH | C564277 | E | validated | |
| UMLS | C1842413 | E | validated | |
| GARD | 10580 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:183666Hyper-IgM syndrome without susceptibility to opportunistic infections
rare genetic diseases; rare immunological diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101091
- This record as JSON: /data/d/101091.json