Phenotype #0000210607

Individual ID 00276051
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Global developmental delay (HP:0001263); Epileptic encephalopathy (HP:0200134); Seizures (HP:0001250); Microcephaly (HP:0000252); Hearing impairment (HP:0000365); Ventriculomegaly (HP:0002119); Agenesis of corpus callosum (HP:0001274); Periventricular leukomalacia (HP:0006970)
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name IMGAG
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by IMGAG
Date created 2020-01-24 11:03:01 +01:00 (CET)
Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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