Disease #01591 (complete trisomy 21 syndrome, OMIM:190685)

Official abbreviation -
Name complete trisomy 21 syndrome
OMIM ID 190685
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GATA1
Associated tissues -
Disease features -
Remarks -

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