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Disease Ontology Browser
hydrolethalus syndrome (DOID:0050779)
Alliance: disease page
Synonyms: Salonen-Herva-Norio syndrome
Alt IDs: OMIM:236680, OMIM:614120, ICD10CM:Q87.8, ORDO:2189
Definition: An autosomal recessive disease characterized by mulitple fetal developmental defects including polydactyly and central nervous system malformations that results from a single amino acid mutation of D211G of the HYLS1 gene which plays a central role in cilia formation.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory