Disease #05457 (SCARMD (dystrophy, muscular, severe autosomal recessive (SCARMD))))

Official abbreviation SCARMD
Name dystrophy, muscular, severe autosomal recessive (SCARMD))
OMIM ID -
Inheritance -
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2018-07-12 09:14:48 +02:00 (CEST)
Date last edited N/A


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00133642 - - - M ? (Italy) - - - - - SCARMD - SGCA SGCB 1 1 Marina Fanin
00133805 - PubMed: Ben Othmane, PubMed: Ben Othmane 1995, PubMed: Noguchi 1995, OMIM:var0001 muscle RNA - - Tunisia - - - - - SCARMD - SGCG SGCG 2 3 Johan den Dunnen
00133833 - PubMed: Noguchi 1995 - - - Japan - - - - - SCARMD - SGCG SGCG 1 1 Johan den Dunnen
00134012 - - - F ? (Italy) white - - - - SCARMD - SGCG SGCG 1 1 Marina Fanin
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