Disease #07103 (CAGS (Chopra-Amiel-Gordon syndrome), OMIM:619504)
Official abbreviation |
CAGS |
Name |
Chopra-Amiel-Gordon syndrome |
OMIM ID |
619504 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
ANKRD17 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2024-09-18 09:51:16 +02:00 (CEST) |
Date last edited |
N/A |
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