Search Ontology:
Human Disease

Meckel syndrome 11

Term ID
DOID:0061296
Synonyms
Definition
A Meckel syndrome that has_material_basis_in homozygous mutation in the TMEM231 gene on chromosome 16q23. https://pubmed.ncbi.nlm.nih.gov/23349226/
References
Ontology
Human Disease   ( DOID:0061296 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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