Disease #00808 (Growth retardation with deafness and mental retardation due to IGF1 deficiency, OMIM:608747)
| Official abbreviation |
- |
| Name |
Growth retardation with deafness and mental retardation due to IGF1 deficiency |
| OMIM ID |
608747 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
IGF1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
