ORPHA:101977
Immunodeficiency due to predominantly antibodies defect
Synonyms: PAD · Predominantly antibodies deficiency
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Immunodeficiency due to predominantly antibodies defect | PAD · Predominantly antibodies deficiency |
| fr | Déficit immunitaire par déficit de production d'anticorps | PAD · Immunodéficience par déficit de production d'anticorps |
| de | Immundefekt durch vorwiegenden Antikörperdefekt | PAD · Vorwiegender Antikörpermangel · Immundefekt mit vorwiegender Beeinträchtigung der Antikörper-Produktion |
| es | Inmunodeficiencia con predominio de defectos de los anticuerpos | Deficiencia predominantemente de anticuerpos |
| it | Immunodeficienza da deficit prevalente degli anticorpi | PAD · Deficit prevalente degli anticorpi |
| nl | Immuundeficiëntie door voornamelijk defect van antilichamen | PAD · Voornamelijk deficiëntie van antilichamen |
| pt | Imunodeficiência afetando predominantemente a produção de anticorpos | |
| pl | Niedobór odporności dotyczący głównie produkcji przeciwciał | = en |
| cs | Imunodeficience postihující převážně produkci protilátek | = en |
| uk | Імунодефіцит, що переважно уражує вироблення антитіл | |
| zh | 主要影响抗体产生的免疫缺陷 | |
| tr | Ağırlıklı antikor üretimini etkileyen immün yetmezlik |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 4A01.0 | E | specific | validated |
| MONDO | 15132 | E | validated | |
| UMLS | C5681776 | 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:179006Primary immunodeficiency due to a defect in adaptive immunity
rare genetic diseases; rare immunological diseases
Children (8):
- ORPHA:183669Agammaglobulinemia
- ORPHA:1006Alopecia antibody deficiency
- ORPHA:696851Common variable immunodeficiency and related disorders
- ORPHA:331232Immunodeficiency with isotype or light chain deficiencies with normal number of B-cells
- ORPHA:331240Immunodeficiency with severe reduction in serum IgG and IgA with normal/elevated IgM and normal number of B-cells
- ORPHA:178389Osteopetrosis-hypogammaglobulinemia syndrome
- ORPHA:3132Say-Barber-Miller syndrome
- ORPHA:169443Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells
Codes that Orphanet moved or referred to this one:
- ORPHA:2621OBSOLETE: Low birth weight-dwarfism-dysgammaglobulinemia syndrome referred to · inactive
- ORPHA:99972OBSOLETE: Immunoglobulin A1 deficiency referred to · inactive
- ORPHA:99973OBSOLETE: Immunoglobulin A2 deficiency referred to · inactive
- ORPHA:101978OBSOLETE: Disease with severe reduction in all serum immunoglobulin isotypes with profoundly decreased or absent B cells referred to · inactive
- ORPHA:331244OBSOLETE: Other immunodeficiency syndrome with predominantly antibody defects referred to · inactive
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/101977
- This record as JSON: /data/d/101977.json