Phenotype #0000276750

Individual ID 00382894
Associated disease -
Phenotype details retinitis pigmentosa (RP), obesity (Ob), polydactyly (PD), developmental delay (Dev), gonadal and renal malformations
Diagnosis/Initial Bardet-Biedl syndrome (BBS)
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 2021-09-13 01:01:20 +02:00 (CEST)
Date last edited N/A

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