Disease #03674 (MRMV2 (mirror movements, type 2 (MRMV-2)), OMIM:614508)

Official abbreviation MRMV2
Name mirror movements, type 2 (MRMV-2)
OMIM ID 614508
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 5
Associated with 1 gene RAD51
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00430899 827 - F no France white - - - - MRMV, MRMV2 - RAD51 RAD51 1 1 Oriane Trouillard
00430900 1326 - - F no France white - - - - MRMV2 - RAD51 RAD51 1 1 Oriane Trouillard
00430901 1374 - - M no Denmark white - - - - MRMV2 - RAD51 RAD51 1 1 Oriane Trouillard
00430984 984 - - M no France white - - - - MRMV2 - RAD51 RAD51 1 1 Oriane Trouillard
00430985 1386 - - F no France white - - - - MRMV2 - RAD51 RAD51 1 1 Oriane Trouillard
00430987 1043 - - F no France white - - - - MRMV2 - RAD51 RAD51 1 1 Oriane Trouillard
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