has material basis in germline mutation in disease has feature CLPB metabolic disease 3-methylglutaconic aciduria, type VIIB https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/3_methylglutaconic_aciduria_neonatal_cataract_neurologic_involvement_congenital_neutropenia_syndrome https://www.malacards.org/card/3_methylglutaconic_aciduria_type_viib https://www.malacards.org/card/3_methylglutaconic_aciduria_with_cataracts_neurologic_involvement_and_neutropenia_2 OMIM:616271 DOID:0081134 MGA7 3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia MEGCANN MEDGEN:1810214 MGCA7 Orphanet:445038 GARD:0017767 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia MONDO:0014561 SCTID:764860006 UMLS:C5676893 3-methylglutaconic aciduria-cataract-neurologic involvement-neutropenia syndrome DOID:0110003 CLPB 3-methylglutaconic aciduria Present because it is in the OMIM series. 3-methylglutaconic aciduria type 7 3-methylglutaconic aciduria