has material basis in germline mutation in
KYNU
congenital vertebral-cardiac-renal anomalies syndrome
vertebral, cardiac, renal, and limb defects syndrome 2
https://github.com/monarch-initiative/mondo/issues/4948
https://github.com/monarch-initiative/mondo/issues/6751
VCRL2
MONDO:0060555
congenital NAD deficiency disorder 2
GARD:18509
This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'musculoskeletal system disorder' (MONDO:0002081) ontology branch (https://orcid.org/0000-0001-9310-0163)
kynureninase deficiency, complete
UMLS:C4540014
OMIM:617661
vertebral, cardiac, renal, and limb defects syndrome 2