Phenotype #0000201820

Individual ID 00263961
Associated disease retinal disease
Phenotype details retinitis pigmentosa (HP:0000510), field constriction (HP: 0007994), atrophy of retinal pigment epithelium (HP:0007722), high myopia (HP:0011003)
Diagnosis/Initial retinitis pigmentosa (RP)
Inheritance Familial, autosomal recessive
Diagnosis/Definite retinitis pigmentosa type 72 (RP-72)
Age/Examination 50y (50 years)
Age/Diagnosis 20y
Age/Onset 17y
Phenotype/Onset night blindness (HP:0000662), field constriction (HP:0007994)
Protein -
Owner name Jasmine Chen