PLA2G6-associated neurodegeneration hereditary peripheral neuropathy neurodegeneration with brain iron accumulation 2A https://rarediseases.info.nih.gov/diseases/2751/hunter-carpenter-macdonald-syndrome MEDGEN:82852 ICD9:330.8 neurodegeneration, PLA2G6-associated Hunter Carpenter Macdonald syndrome infantile neuroaxonal dystrophy/atypical neuroaxonal dystrophy PLAN neurodegeneration with brain iron accumulation 2A GARD:0003957 Orphanet:35069 neurodegeneration with brain iron accumulation type 2a NANDO:1200537 neuroaxonal dystrophy presenting with neonatal dysmorphic features, early onset of peripheral gangrene NBIA2a phospholipase A2-associated neurodegeneration neurodegeneration, Pla2G6-associated MONDO:0024457 SCTID:52713000 INAD AR PLA2G6 NCIT:C84927 INAD1 NBIA2A UMLS:C0270724 MESH:C536071 DOID:0110735 Hunter-Carpenter-McDonald syndrome inaD KARAK syndrome, included infantile neuroaxonal dystrophy neurodegeneration with brain iron accumulation type 2A Seitelberger disease neurodegeneration, Pla2g6-associated OMIM:256600