Disease #04368 (CAPOS (CAPOS syndrome (CAPOS)), OMIM:601338)

Official abbreviation CAPOS
Name CAPOS syndrome (CAPOS)
OMIM ID 601338
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ATP1A3
Associated tissues -
Disease features -
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Individuals

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00080942 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - 0 - - CAPOS CAPOS syndrome (OMIM:601338) ATP1A3 ATP1A3 1 1 Daniel Trujillano
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