Phenotype #0000319106

Individual ID 00428194
Associated disease RSTS1
Phenotype details Global developmental delay, Autistic behavior, Unilateral renal agenesis, Esophageal atresia, Sleep disturbance, Impaired social interactions, Constipation, Hyperactivity, Delayed speech and language development, high forehead, backward rotated ears, corners of the mouth turned downwards
Diagnosis/Initial -
Inheritance Unknown
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 2022-12-23 15:00:57 +01:00 (CET)
Date last edited 2023-01-13 09:48:53 +01:00 (CET)

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