Disease #03035 (OPTB6 (osteopetrosis, autosomal recessive, type 6 (OPTB-6)), OMIM:611497)
Official abbreviation |
OPTB6 |
Name |
osteopetrosis, autosomal recessive, type 6 (OPTB-6) |
OMIM ID |
611497 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PLEKHM1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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