Disease #00045

Official abbreviation 613076
Name Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay, 613076 (3)
OMIM ID 613076
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GFER
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 21
LOVD software ©2004-2018 Leiden University Medical Center