PROM1, prominin 1, 8842

N. diseases: 477; N. variants: 33
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		0.800 CausalMutation disease CLINVAR
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		0.800 Biomarker disease CTD_human
CUI: C2677516
Disease: RETINITIS PIGMENTOSA 41 (disorder)
RETINITIS PIGMENTOSA 41 (disorder) 		0.800 GeneticVariation disease CLINVAR
CUI: C1863534
Disease: Stargardt disease 4
Stargardt disease 4 		0.720 CausalMutation disease CLINVAR
CUI: C1863534
Disease: Stargardt disease 4
Stargardt disease 4 		0.720 Biomarker disease CTD_human
CUI: C1863534
Disease: Stargardt disease 4
Stargardt disease 4 		0.720 Biomarker disease GENOMICS_ENGLAND
CUI: C1863534
Disease: Stargardt disease 4
Stargardt disease 4 		0.720 Biomarker disease GENOMICS_ENGLAND
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy 		0.700 Biomarker disease CTD_human
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0339512
Disease: Bull's eye macular dystrophy
Bull's eye macular dystrophy 		0.700 CausalMutation disease CLINVAR
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		0.700 Biomarker disease CTD_human
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		0.700 CausalMutation disease CLINVAR
CUI: C2675210
Disease: CONE-ROD DYSTROPHY 12 (disorder)
CONE-ROD DYSTROPHY 12 (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.440 Biomarker disease GENOMICS_ENGLAND
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.440 GeneticVariation disease CLINVAR
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.300 Biomarker group GENOMICS_ENGLAND
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.300 Biomarker group GENOMICS_ENGLAND
CUI: C0015397
Disease: Disorder of eye
Disorder of eye 		0.300 Biomarker group GENOMICS_ENGLAND
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		0.190 Biomarker disease HPO
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		0.180 CausalMutation disease CLINVAR