Disease #04568 (AYGRP (Ayme-Gripp syndrome (AYGRP)), OMIM:601088)
Official abbreviation |
AYGRP |
Name |
Ayme-Gripp syndrome (AYGRP) |
OMIM ID |
601088 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
MAF |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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