Phenotype #0000273598

Individual ID 00379744
Associated disease CHM
Phenotype details HP:0032037, HP:0000662, HP:0001123, HP:0001417, HP:0001139
Diagnosis/Initial choroideremia (CHM)
Inheritance Familial, X-linked dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Jinu Han
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Jinu Han
Date created 2021-08-09 03:38:59 +02:00 (CEST)
Date last edited 2021-08-09 09:27:21 +02:00 (CEST)

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