OBO ID: DOID:0080517
Term Name: Meier-Gorlin syndrome 6 Search Ontology:
Synonyms:
Definition: A Meier-Gorlin syndrome that has_material_basis_in heterozygous mutation in the GMNN gene on chromosome 6p22. https://www.omim.org/entry/616835
References:
Ontology: Human Disease   ( DOID:0080517 )
Relationships
is a type of:
OTHER Meier-Gorlin syndrome 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GMNN Meier-Gorlin syndrome 6 616835
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.