Phenotype #0000239722

Individual ID 00315977
Associated disease ?
Diagnosis/Initial neurodevelopmental delay
Diagnosis/Definite -
Phenotype details see paper; ..., no failure to thrive; no globe defect; no coloboma; visual impairment; Esotropia; nystagmus; motor delay; speech delay; no behavioral features; no hypotonia; cardiac defect; kidney anomaly; Low-set ears; bilateral epicanthal folds; obstructive sleep apnea
Inheritance Isolated (sporadic)
Age/Examination 04y07m (4 years, 7 months)
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 2020-11-01 10:06:29 +01:00 (CET)
Date last edited 2022-11-30 19:32:28 +01:00 (CET)

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