Phenotype #0000268810

Individual ID 00373536
Associated disease NEDSWMA;CPSQ1
Diagnosis/Initial -
Diagnosis/Definite Neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities (OMIM 618994)
Phenotype details HP:0002353; HP:0002539; HP:0002079; HP:0003155; HP:0012704; HP:0001263; HP:0001250; HP:0001276
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Wenjuan Qiu
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Wenjuan Qiu
Date created 2021-05-17 10:08:42 +02:00 (CEST)
Date last edited 2021-05-28 13:27:06 +02:00 (CEST)

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