Search Ontology:
Human Disease

hydrolethalus syndrome 2

Term ID
DOID:0111356
Synonyms
  • HLS2
Definition
A hydrolethalus syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KIF7 gene on chromosome 15q26.1. https://www.ncbi.nlm.nih.gov/pubmed/21552264
References
Ontology
Human Disease   ( DOID:0111356 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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