OBO ID: DOID:0111355 |
Term Name: | hydrolethalus syndrome 1 | Search Ontology: | |
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Definition: | A hydrolethalus syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the HYLS1 gene on chromosome 11q24.2. https://www.ncbi.nlm.nih.gov/pubmed/15843405 | ||
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Ontology: | Human Disease ( DOID:0111355 ) |
OTHER hydrolethalus syndrome 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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