Disease #01684 (bulbar palsy of childhood, progressive, OMIM:211500)

Official abbreviation -
Name bulbar palsy of childhood, progressive
OMIM ID 211500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 0 genes -
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Individuals

1 entry on 1 page. Showing entry 1.
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00080886 - Trujillano et al., submitted unaffected parents - - - - - 0 - - bulbar palsy of childhood, progressive Fazio-Londe disease (OMIM:211500) SLC52A3 SLC52A3 1 1 Daniel Trujillano
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