Phenotype #0000223949

Individual ID 00296542
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details Abnormal CNS myelination (HP:0011400); Global developmental delay (HP:0001263); Abnormality of nervous system physiology (HP:0012638); Leukodystrophy (HP:0002415); Hyperopic astigmatism (HP:0000484); Abnormality of refraction (HP:0000539)
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 2020-04-08 09:52:01 +02:00 (CEST)
Date last edited 2020-07-20 09:43:51 +02:00 (CEST)

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