Disease #05570 (SLI5 (language impairment, specific, type 5 (SLI-5)), OMIM:615432)
| Official abbreviation |
SLI5 |
| Name |
language impairment, specific, type 5 (SLI-5) |
| OMIM ID |
615432 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TM4SF20 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2019-02-14 16:23:00 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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