Disease #05681 (VCRL1 (vertebral, cardiac, renal, and limb defects syndrome, type 1 (VCRL1)), OMIM:617660)

Official abbreviation VCRL1
Name vertebral, cardiac, renal, and limb defects syndrome, type 1 (VCRL1)
OMIM ID 617660
Human Phenotype Ontology Project (HPO) HPO
Inheritance AR
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HAAO
Associated tissues -
Disease features -
Remarks -