Phenotype #0000207732

Individual ID 00269936
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Hypospadias (HP:0000047); Microcephaly (HP:0000252); Epicanthus (HP:0000286); Strabismus (HP:0000486); Myopia (HP:0000545); Delayed speech and language development (HP:0000750); Seizures (HP:0001250); Global developmental delay (HP:0001263); Agenesis of corpus callosum (HP:0001274); Dandy-Walker malformation (HP:0001305); Polymicrogyria (HP:0002126); Gait imbalance (HP:0002141); Abnormality of mouth size (HP:0011337)
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 2019-12-10 12:34:09 +01:00 (CET)
Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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