Disease #01362

Official abbreviation FHM-1
Name migraine, hemiplegic, familial, type 1 (FHM-1)
OMIM ID 141500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 1
Associated with 1 gene CACNA1A
Associated tissues -
Disease features -
Remarks -


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00110576 - - - - - (Germany) - - 0 - - FHM-1 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00110584 - - - - - (Germany) - - 0 - - FHM-1 - CACNA1A CACNA1A 2 1 Birgit Neitzel
00110590 - - - - - (Germany) - - 0 - - FHM-1 - CACNA1A CACNA1A 1 1 Birgit Neitzel
00110594 - - - - - (Germany) - - 0 - - FHM-1 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 - - - - - 0 - - FHM-1 - CACNA1A - 0 1 Elles Boon
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