Disease #00018 (PKD (Paroxysmal kinesigenic dyskinesia))

Official abbreviation PKD
Name Paroxysmal kinesigenic dyskinesia
OMIM ID -
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 2 genes PRRT2, TMEM151A
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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Owner     
00002117 - - - - - - PKD paroxysmak kinesigenic dyskinesia TMEM151A TMEM151A 1 2 Yulan Chen
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