Disease #02535

Official abbreviation CHN
Name neuropathy, hypomyelinating, congenital (CHN)
OMIM ID 605253
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 2 genes EGR2, MPZ
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00063715 - PubMed: McMillan 2010 - - - - - - 0 - - CHN - MPZ MPZ 1 1 Johan den Dunnen
00063726 - PubMed: McMillan 2010 - - - - - - 0 - - CHN - MPZ MPZ 1 1 Johan den Dunnen
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