Phenotype #0000308328

Individual ID 00416608
Associated disease CPCMR
Diagnosis/Initial 1y
Diagnosis/Definite -
Phenotype details Ventricular septal defect, Hypotonia, Motor delay, Expressive language delay, Pes planus, Gait ataxia, Neurodevelopmental abnormality, Impaired social interactions, Sleep disturbance, Delayed speech and language development, Genu valgum, Short stature
Inheritance Isolated (sporadic)
Age/Examination -
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 2022-09-06 11:07:02 +02:00 (CEST)
Date last edited 2022-09-06 15:14:42 +02:00 (CEST)

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