Disease #05236 (HMLR2 (syndrome, Heimler, type 2 (HMLR2)), OMIM:616617)
Official abbreviation |
HMLR2 |
Name |
syndrome, Heimler, type 2 (HMLR2) |
OMIM ID |
616617 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
AR |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 1 gene |
PEX6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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