Phenotype #0000312188

Individual ID 00420948
Associated disease MRXSSB
Phenotype details Global developmental delay, Axial hypotonia, Microcephaly, Dyskinesia
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 01y (1 year)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Andreas Laner
Date created 2022-11-03 14:09:17 +01:00 (CET)
Date last edited 2022-11-04 12:15:48 +01:00 (CET)

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