Disease #05059

Official abbreviation CTRCT-43
Name cataract?, type 43 (CTRCT-43)
OMIM ID 616279
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene UNC45B
Associated tissues -
Disease features -
Remarks -