Search Ontology:
Human Disease

Meier-Gorlin syndrome 6

Term ID
DOID:0080517
Synonyms
Definition
A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22. https://pubmed.ncbi.nlm.nih.gov/26637980/
References
Ontology
Human Disease   ( DOID:0080517 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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