Phenotype #0000337084

Individual ID 00447892
Associated disease LAMSHF
Phenotype details Neurodevelopmental delay, Motor delay, Hypotonia, Elevated circulating creatine kinase concentration, Facial asymmetry
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 02y (2 years)
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 2024-01-31 13:41:43 +01:00 (CET)
Date last edited 2024-01-31 15:19:38 +01:00 (CET)

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