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Parent Node:
expandrare hereditary disease with peripheral neuropathy (MONDO:0016132)
..Starting node
..expandrare hereditary metabolic disease with peripheral neuropathy ()

       Child Nodes:
........expandabetalipoproteinemia ()
........expandadrenomyeloneuropathy ()
........expandadult polyglucosan body disease ()
........expandadult Refsum disease ()
........expandbeta-mannosidosis ()
........expandbiotinidase deficiency ()
........expandcataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome ()
........expandcerebrotendinous xanthomatosis ()
........expandchorea-acanthocytosis ()
........expandcongenital bile acid synthesis defect 4 ()
........expandde Barsy syndrome ()
........expandFabry disease ()
........expandfamilial isolated deficiency of vitamin E ()
........expandgyrate atrophy ()
........expandhomocystinuria due to methylene tetrahydrofolate reductase deficiency ()
........expandKrabbe disease ()
........expandLeigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome ()  LSDB  L: 00525;
........expandlong chain 3-hydroxyacyl-CoA dehydrogenase deficiency ()  LSDB  L: 00474;
........expandmetachromatic leukodystrophy ()
........expandmethylmalonic aciduria and homocystinuria type cblC ()
........expandmitochondrial disease with peripheral neuropathy ()
........expandNiemann-Pick disease type B ()
........expandnon-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy ()
........expandoptic atrophy-peripheral neuropathy-developmental delay syndrome ()
........expandperoxisome biogenesis disorder ()
........expandSandhoff disease ()
........expandTangier disease ()
........expandTay-Sachs disease ()
........expandtyrosinemia type I ()
........expandWilson disease ()



 Sister Nodes: 
..expandattenuated ChC)diak-Higashi syndrome ()
..expandChediak-Higashi syndrome ()
..expandPHARC syndrome ()
..expandrare hereditary metabolic disease with peripheral neuropathy ()
..expandrare hereditary neurologic disease with peripheral neuropathy ()
..expandrare hereditary systemic disease with peripheral neuropathy ()
..expandtriple-A syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:16133
Name:rare hereditary metabolic disease with peripheral neuropathy
Definition:
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Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
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Phenotypes
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