Disease #05677 (SNIBCPS (Snijders Blok-Campeau syndrome), OMIM:618205)
| Official abbreviation |
SNIBCPS |
| Name |
Snijders Blok-Campeau syndrome |
| OMIM ID |
618205 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
4 |
| Phenotype entries for this disease |
4 |
| Associated with 1 gene |
CHD3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2019-12-28 20:08:02 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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