ORPHA:101104
Marin-Amat syndrome
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- active
This disease is described under Marcus-Gunn syndrome
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Marin-Amat syndrome | |
| fr | Syndrome de Marin-Amat | |
| de | Marin-Amat-Syndrom | |
| es | Síndrome de Marin-Amat | |
| it | Sindrome di Marin-Amat | |
| nl | Marin-Amatsyndroom | |
| pt | Síndrome Marin-Amat | |
| pl | Zespół Marina i Amata | |
| cs | Marin-Amatův syndrom | |
| uk | Синдром Марін-Амата | |
| zh | Marin-Amat 综合征 | |
| tr | Marin-Amat sendromu |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | Q07.8 | NTBT | attributed | validated |
| ICD-11 | 9A03.00 | NTBT | index | validated |
| MONDO | 0015101 | E | validated | |
| UMLS | C5681802 | E | validated | |
| GARD | 19779 | 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:91412Marcus-Gunn syndrome
rare developmental anomalies during embryogenesis; rare genetic diseases; rare ophthalmic 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/101104
- This record as JSON: /data/d/101104.json