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

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