Phenotypes for disease #06870 (HPE13 (Holoprosencephaly 13, X-linked), OMIM:301043)

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AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000351320 - - Abnormality of prenatal development or birth, Spina bifida, Abnormal heart morphology, Abnormal fetal cardiovascular morphology, Single ventricle Isolated (sporadic) 00y00m25w - - - Andreas Laner 00465874
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