Phenotype #0000186487

Individual ID 00246631
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details HP:0010952 (Mild fetal ventriculomegaly); HP:0001331 (Absent septum pellucidum); HP:0002119 (Ventriculomegaly); HP:0001197 (Abnormality of prenatal development or birth)
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2019-07-15 17:47:29 +02:00 (CEST)
Date last edited 2019-07-16 07:18:39 +02:00 (CEST)

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