Disease #05569 (SPCH1 (speech-language disorder, type 1 (SPCH-1)), OMIM:602081)
| Official abbreviation |
SPCH1 |
| Name |
speech-language disorder, type 1 (SPCH-1) |
| OMIM ID |
602081 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
FOXP2 |
| Associated tissues |
- |
| Disease features |
autosomal dominant |
| Remarks |
- |
| Date created |
2019-02-14 16:20:26 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|