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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
disorder of sialic acid metabolism +  
glycoprotein storage disease 
glycoproteinosis +  
hereditary spastic paraplegia 48 
inborn disorder of lysosomal amino acid transport +  
late infantile neuronal ceroid lipofuscinosis +  
lysosomal acid phosphatase deficiency 
lysosomal glycogen storage disease +  
lysosomal lipid storage disorder +   
mucopolysaccharidosis +  
pycnodysostosis 

Synonyms
Alternate IDs: MONDO:0017736
Xrefs: GARD:21332 ;   ICD9:277.89 ;   MEDGEN:575253 ;   ORDO:309319 ;   SCTID:238050009 ;   UMLS:C0342851 ;   icd11.foundation:1709765980

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