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Unexplained young onset end-stage renal disease - additional genes v0.93 HPSE2 Achchuthan Shanmugasundram Phenotypes for gene: HPSE2 were changed from Urofacial Syndrome; Urofacial syndrome 1 236730; Congenital bladder disease: dyssynergic, high pressure bladder to Urofacial syndrome 1, OMIM:236730; Congenital bladder disease: dyssynergic, high pressure bladder
Unexplained young onset end-stage renal disease - additional genes v0.68 HPSE2 Achchuthan Shanmugasundram Added phenotypes Urofacial Syndrome; Urofacial syndrome 1 236730; Congenital bladder disease: dyssynergic, high pressure bladder for gene: HPSE2
Publications for gene: HPSE2 were updated from 20560210; 20560209 to 20560209; 20560210
Unexplained young onset end-stage renal disease - additional genes v0.65 HPSE2 Achchuthan Shanmugasundram reviewed gene: HPSE2: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Unexplained young onset end-stage renal disease - additional genes v0.53 HPSE2 Achchuthan Shanmugasundram Entity copied from Unexplained young onset end-stage renal disease v5.32
Unexplained young onset end-stage renal disease - additional genes v0.53 HPSE2 Achchuthan Shanmugasundram gene: HPSE2 was added
gene: HPSE2 was added to Unexplained young onset end-stage renal disease - additional genes. Sources: Expert Review Green
Mode of inheritance for gene: HPSE2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: HPSE2 were set to 20560210; 20560209
Phenotypes for gene: HPSE2 were set to Congenital bladder disease: dyssynergic, high pressure bladder; Urofacial syndrome 1 236730; Urofacial Syndrome