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 Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00080886 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - bulbar palsy of childhood, progressive Fazio-Londe disease (OMIM:211500) SLC52A3 SLC52A3 1 1 Daniel Trujillano
00409541 K6644 PubMed: Oishi 2018 - F - Japan - - - - - bulbar palsy of childhood, progressive best corrected visual acuity: 1.2; electroretinogram , rod: mildly reduced, cone: mildly reduced CYP4V2 CYP4V2 2 1 LOVD
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