Phenotype #0000337401

Individual ID 00448191
Associated disease ?
Diagnosis/Initial rare disorder
Diagnosis/Definite -
Phenotype details motor delay; hearing impairment; strabismus; laryngomalacia; umbilical hernia; skeletal anomalies; dysmorphic facial features
Inheritance Isolated (sporadic)
Age/Examination 12y (12 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-02-22 17:47:06 +01:00 (CET)
Date last edited N/A

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