ORPHA:169110
Immunoglobulin heavy chain deficiency
- Type
- Disease
- Group
- Disorder
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Immunoglobulin heavy chain deficiency | |
| fr | Déficit en chaîne lourde des immunoglobulines | |
| de | Defekt der schweren Immunglobulinkette | |
| es | Deficiencia de cadenas pesadas de inmunoglobulinas | |
| it | Deficit della catena pesante dell'immunoglobulina | |
| nl | Deficiëntie van zware keten van immunoglobuline | |
| pt | Deficiência de cadeias pesadas da imunoglobulina | |
| pl | Niedobór łańcuchów ciężkich immunoglobulin | |
| cs | Deficit těžkého řetězce imunoglobulinu | |
| uk | Дефіцит важкого ланцюга імуноглобуліну | |
| zh | 免疫球蛋白重链缺陷 | |
| tr | İmmünoglobulin ağır zincir eksikliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D80.8 | NTBT | attributed | validated |
| ICD-11 | 4A01.04 | NTBT | index | validated |
| MONDO | 0015697 | E | validated | |
| UMLS | C0398692 | 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:331232Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells
rare genetic diseases; rare immunological diseases
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/169110
- This record as JSON: /data/d/169110.json