ORPHA:98604
Congenital alacrima
- 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 | Congenital alacrima | |
| fr | Alacrymie congénitale | |
| de | Alakrimie, kongenitale | |
| es | Alacrima congénita | |
| it | Alacrimia congenita | |
| nl | Congenitale alacrimie | |
| pt | Alacrima congénita | |
| pl | Wrodzony brak łez | |
| cs | Vrozená alacrima | |
| uk | Вроджена алакрімія | |
| zh | 先天性无泪症 | |
| tr | Doğumsal alakrima |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C566307 | E | validated | |
| UMLS | C1863199 | 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 (2):
- ORPHA:98602Rare disorder of the lacrimal apparatus
rare ophthalmic disorders - ORPHA:522532Rare genetic disorder of the lacrimal apparatus
rare genetic diseases
Children (9):
- ORPHA:404454Alacrimia-choreoathetosis-liver dysfunction syndrome
- ORPHA:86815Aplasia of lacrimal and salivary glands
- ORPHA:1764Familial dysautonomia
- ORPHA:528105Hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome
- ORPHA:238468Hypohidrotic ectodermal dysplasia
- ORPHA:98813Hypohidrotic ectodermal dysplasia with immunodeficiency
- ORPHA:289483Intellectual disability-alacrima-achalasia syndrome
- ORPHA:91416Isolated congenital alacrima
- ORPHA:869Triple A syndrome
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/98604
- This record as JSON: /data/d/98604.json