Disease #00791 (MRT12 (mental retardation, autosomal recessive, type 12 (MRT-12)), OMIM:611090)

Official abbreviation MRT12
Name mental retardation, autosomal recessive, type 12 (MRT-12)
OMIM ID 611090
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene ST3GAL3
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00155024 21907012-FamM096 PubMed: Hu 2011 6-generation family, 8 affecteds (4F, 4M), unaffected heterozygous carrier parents F;M yes Iran - - 0 - - MRT12 see paper; ... - ST3GAL3 1 8 Andreas Kuss
00155026 21907012-FamM319 PubMed: Hu 2011 2-generation family, 4 affected (F, 3M), unaffected heterozygous carrier parents/relatives F;M yes Iran - - 0 - - MRT12 see paper; ... - ST3GAL3 1 4 Andreas Kuss
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