Disease #01362 (FHM1 (migraine, hemiplegic, familial, type 1), OMIM:141500)

Official abbreviation FHM1
Name migraine, hemiplegic, familial, type 1
OMIM ID 141500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 3
Associated with 1 gene CACNA1A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2023-03-22 16:52:54 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00110576 - - - - - (Germany) - - - - - FHM1 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00110584 - - - - - (Germany) - - - - - FHM1 - CACNA1A CACNA1A 2 1 Birgit Neitzel
00110590 - - - - - (Germany) - - - - - FHM1 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00110594 - - - - - (Germany) - - - - - FHM1 passing right-sided hemisymptomatics with aphasia and headache, later on progressing loss of memory and disturbances of equilibrium; mother suffers from regular migraine attacks; twin brother shows peculiar nature, gait and speech CACNA1A CACNA1A 1 1 Birgit Neitzel
00110635 - PubMed: Ducros 2001 1 family - - - - - - - - FHM1 - CACNA1A - - 1 Elles Boon
00239984 - - - M no Italy - 12y - - - FHM1 - ATP1A1, ATP1A2, ATP1A3, ATP1A4, CACNA1A, PRRT2, SCN1A, SLC1A4, SLC4A4 ATP1A4 1 1 Pietro Palumbo
00324119 172661 - - F ? Turkey - - - - - FHM1 one year old patient with tonic upward-looking CACNA1A CACNA1A 1 1 Andreas Laner
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