cataract 38

Term ID

DOID:0110245

Synonyms

• autosomal recessive congenital cataract 5
• CATC5
• CTRCT38

Definition

A cataract that has_material_basis_in homozygous mutation in the AGK gene on chromosome 7q34. https://www.ncbi.nlm.nih.gov/pubmed/22415731

References

• ICD10CM:Q12.0
• OMIM:614691

Ontology

Human Disease   ( DOID:0110245 )