Phenotype #0000337846

Individual ID 00448669
Associated disease DD
Phenotype details neurodevelopmental disorder without features of VLDLR cerebellar hypoplasia
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Tess Holling
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Tess Holling
Date created 2024-04-10 10:39:20 +02:00 (CEST)
Date last edited 2024-04-10 11:25:33 +02:00 (CEST)

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