Phenotype #0000227009

Individual ID 00299704
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Macrocephaly (HP:0000256); Global developmental delay (HP:0001263); Abnormality of movement (HP:0100022)
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 2020-04-20 10:40:01 +02:00 (CEST)
Date last edited 2020-05-03 14:51:59 +02:00 (CEST)

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