Disease #06870 (HPE13 (Holoprosencephaly 13, X-linked), OMIM:301043)

Official abbreviation HPE13
Name Holoprosencephaly 13, X-linked
OMIM ID 301043
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene STAG2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00465874 334050 - prenatal Dx F no ? (unknown) - - - - - HPE13 Abnormality of prenatal development or birth, Spina bifida, Abnormal heart morphology, Abnormal fetal cardiovascular morphology, Single ventricle STAG2 STAG2 1 1 Andreas Laner
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