Disease #00734 (HYPP (paralysis, periodic, hyperkalemic (HYPP)), OMIM:170500)

Official abbreviation HYPP
Name paralysis, periodic, hyperkalemic (HYPP)
OMIM ID 170500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene SCN4A
Associated tissues -
Disease features autosomal dominant
Remarks -


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00112918 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 3 1 Vincent Janmaat
00112927 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 2 1 Vincent Janmaat
00112931 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 4 1 Vincent Janmaat
00112932 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 3 1 Vincent Janmaat
00112943 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 5 1 Vincent Janmaat
00112992 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 3 1 Vincent Janmaat
00113011 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 3 1 Vincent Janmaat
00113085 - Leiden, unpublished - - - Netherlands - - 0 - - HYPP - SCN4A SCN4A 2 1 Vincent Janmaat
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