Phenotype #0000279078

Individual ID 00385282
Associated disease -
Phenotype details obesity, retinitis pigmentosa, polydactyly, hypogenitalism,mental retardation, anemia HTA
Diagnosis/Initial Bardet–Biedl Syndrome (BBS)
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 6y (6 years)
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 2021-10-09 03:44:00 +02:00 (CEST)
Date last edited N/A

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