Disease #00919 (Sudden infant death with dysgenesis of the testes syndrome, OMIM:608800)

Official abbreviation -
Name Sudden infant death with dysgenesis of the testes syndrome
OMIM ID 608800
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene TSPYL1
Associated tissues -
Disease features -
Remarks -

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