Disease #00579 (AO-1 (atelosteogenesis, type I (AO-1)), OMIM:108720)
Official abbreviation |
AO-1 |
Name |
atelosteogenesis, type I (AO-1) |
OMIM ID |
108720 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
31 |
Phenotype entries for this disease |
7 |
Associated with 1 gene |
FLNB |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
|
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