Disease #00003 (MSX1 (Msh homeobox 1 gene), OMIM:142983)

Official abbreviation MSX1
Name Msh homeobox 1 gene
OMIM ID 142983
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 0 genes -
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Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
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00000023 Salahshourifar I; et al. (2011) - - - - - - MSX1 - MSX1 MSX1 1 1 MyHVP
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