Phenotype #0000304211

Individual ID 00412197
Associated disease NHS
Phenotype details Developmental cataract, Abnormality of eye movement, Nystagmus, Hypospadias, Motor delay, Amblyopia, Global developmental delay
Diagnosis/Initial 0y
Inheritance Familial, X-linked dominant
Diagnosis/Definite -
Age/Examination -
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 2022-06-23 17:05:06 +02:00 (CEST)
Date last edited 2022-06-24 17:36:49 +02:00 (CEST)

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