Disease #00105 (ACG1B (achondrogenesis, type IB (ACG-1B)), OMIM:600972)
| Official abbreviation |
ACG1B |
| Name |
achondrogenesis, type IB (ACG-1B) |
| OMIM ID |
600972 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
3 |
| Associated with 1 gene |
SLC26A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-01-22 07:36:14 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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