Phenotype #0000273622

Individual ID 00379768
Associated disease ACHM
Phenotype details HP:0001141, HP:0000613, HP:0001129, HP:0000639, HP:0000551, HP:0011516
Diagnosis/Initial achromatopsia (ACHM)
Inheritance Familial, autosomal recessive
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 07:02:44 +02:00 (CEST)
Date last edited 2021-08-11 14:36:59 +02:00 (CEST)

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