Phenotype #0000310071

Individual ID 00418775
Associated disease SGS
Phenotype details mitral valve prolapse, aneurismatic ovale fossa, megalocornea, joint hypermobility, Intellectual disability
Diagnosis/Initial Aortic valvular disease
Inheritance Familial
Diagnosis/Definite Shprintzen–Goldberg Syndrome
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Carmela Fusco
Database submission license No license selected
Created by Carmela Fusco
Date created 2022-10-06 13:44:12 +02:00 (CEST)
Date last edited 2022-10-07 10:42:40 +02:00 (CEST)

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