Phenotype #0000323702

Individual ID 00433155
Associated disease CDLS1
Phenotype details microcephaly (HP:0000252) Neurodevelopmental delay, Secundum atrial septal defect, Vesicoureteral reflux, Premature birth, Short stature, Esotropia, Myopia; delayed growth (HP:00001510)
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination 02y (2 years)
Age/Diagnosis -
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 2023-03-01 21:14:39 +01:00 (CET)
Date last edited 2023-03-03 15:00:35 +01:00 (CET)

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