Disease #00303 (HLS2 (hydrolethalus syndrome, type 2 (HLS-2)), OMIM:614120)

Official abbreviation HLS2
Name hydrolethalus syndrome, type 2 (HLS-2)
OMIM ID 614120
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene KIF7
Associated tissues -
Disease features -
Remarks -
Date created 2014-01-19 11:56:48 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00004277 - PubMed: Putoux 2011 - ? ? - - - - - - HLS2 - KIF7 KIF7 1 1 Tania Attie-Bitach
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