Phenotype #0000326593

Individual ID 00436412
Associated disease DEE11
Phenotype details Severe global developmental delay, Microcephaly, Hypertelorism, Long palpebral fissure
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 2023-09-14 13:04:55 +02:00 (CEST)
Date last edited 2023-09-15 10:29:14 +02:00 (CEST)

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