peroxisome biogenesis disorder type 3B
Human disease
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peroxisome biogenesis disorder type 3B
Summary
peroxisome biogenesis disorder type 3B is a class of disease[1].
Key Facts
- peroxisome biogenesis disorder type 3B's instance of is recorded as class of disease[2].
- peroxisome biogenesis disorder type 3B is a type of peroxisomal disease[3].
- peroxisome biogenesis disorder type 3B is a type of Zellweger spectrum disorder[4].
- peroxisome biogenesis disorder type 3B is a type of infantile Refsum disease[5].
- peroxisome biogenesis disorder type 3B is a type of Neonatal adrenoleukodystrophy[6].
- peroxisome biogenesis disorder type 3B's symptoms and signs is recorded as hepatosplenomegaly[7].
- peroxisome biogenesis disorder type 3B's NCI Thesaurus ID is recorded as C84789[8].
- peroxisome biogenesis disorder type 3B's NCI Thesaurus ID is recorded as C155753[9].
- peroxisome biogenesis disorder type 3B's health specialty is recorded as neurology[10].
- peroxisome biogenesis disorder type 3B's genetic association is recorded as PEX12[11].
- peroxisome biogenesis disorder type 3B's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050444[12].
- peroxisome biogenesis disorder type 3B's exact match is recorded as http://identifiers.org/doid/DOID:0050444[13].
- peroxisome biogenesis disorder type 3B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_44[14].
- peroxisome biogenesis disorder type 3B's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_772[15].
- peroxisome biogenesis disorder type 3B's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].