Phenotype #0000161615

Individual ID 00213138
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Global developmental delay (HP:0001263); Muscular hypotonia (HP:0001252); Delayed myelination (HP:0012448); Secundum atrial septal defect (HP:0001684); Poor coordination (HP:0002370)
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 2019-01-11 11:18:46 +01:00 (CET)
Date last edited 2020-04-01 13:57:49 +02:00 (CEST)

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