Phenotype #0000305211

Individual ID 00413230
Associated disease ?
Diagnosis/Initial psychomotor development delay, speech disorders, hypotony, sensory integration disorders
Diagnosis/Definite NEDMIGS
Phenotype details see paper; ...
Inheritance Familial, autosomal recessive
Age/Examination -
Age/Diagnosis 10y
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Rafał Płoski
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Rafał Płoski
Date created 2022-07-12 16:01:20 +02:00 (CEST)
Date last edited 2025-07-23 10:28:35 +02:00 (CEST)

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