Disease #04629 (ICCA (convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA)), OMIM:602066)

Official abbreviation ICCA
Name convulsions, familial infantile, with paroxysmal choreoathetosis (ICCA)
OMIM ID 602066
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 6
Associated with 1 gene PRRT2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00107926 - PubMed: Heron 2012 - - - - - - - - - ICCA - PRRT2 PRRT2 1 1 SIB - Livia Famiglietti
00153280 - - - F - Netherlands white - - - - ICCA - - PRRT2 1 1 Danique Vlaskamp
00153283 - - - F - Netherlands white - - - - ICCA - - PRRT2 1 1 Danique Vlaskamp
00207573 - - - M - China White 02y - yes carbamazepine ICCA HP:0001332, HP:0002305, HP:0001250, HP:0002076, HP:0002356, HP:0100660, HP:0002072, HP:0004305, HP:0011157 PRRT2 PRRT2 4 1 Zhu Jin Ling
00207574 - - - M ? China White 00y04m - yes - ICCA HP:0001332 HP:0002305 HP:0001250 HP:0002356 HP:0100660 HP:0002072 HP:0004305 HP:0011157 HP:0002076 PRRT2 PRRT2 1 2 Zhu Jin Ling
00207717 - - - F - China - 00y04m - - - ICCA - PRRT2 PRRT2 1 1 Zhu Jin Ling
00331292 175351 - - M ? Germany - - - - - ICCA (+) Paroxysmal dyskinesia,(+) Dyskinesia PRRT2 PRRT2 1 1 Andreas Laner
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