Phenotype #0000278582

Individual ID 00384799
Associated disease -
Phenotype details obesity, mental retardation, polydactyly, typical facies, bicuspid aortic valve, hypogenitalism
Diagnosis/Initial Retinitis pigmentosa (RP)
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2021-10-05 15:28:49 +02:00 (CEST)
Date last edited N/A

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