Phenotype #0000283605

Individual ID 00390066
Associated disease ?
Diagnosis/Initial -
Diagnosis/Definite -
Phenotype details global developmental delay, intellectual disability, camptodactyly, upslanting palpebral fissures, microstomia, coloboma, sparse hair
Inheritance Isolated (sporadic)
Age/Examination 3y (3 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 2021-11-09 16:34:00 +01:00 (CET)
Date last edited N/A

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