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 Autosomal recessive
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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