Disease: Renal Hypodysplasia, Nonsyndromic, 1 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1835826
Disease: Renal Hypodysplasia, Nonsyndromic, 1
Renal Hypodysplasia, Nonsyndromic, 1 		0.700 Biomarker disease GENOMICS_ENGLAND Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23. 28157540 2017
CUI: C1835826
Disease: Renal Hypodysplasia, Nonsyndromic, 1
Renal Hypodysplasia, Nonsyndromic, 1 		0.700 Biomarker disease GENOMICS_ENGLAND Large Intragenic Deletion in DSTYK Underlies Autosomal-Recessive Complicated Spastic Paraparesis, SPG23. 28157540 2017
CUI: C1835826
Disease: Renal Hypodysplasia, Nonsyndromic, 1
Renal Hypodysplasia, Nonsyndromic, 1 		0.700 GeneticVariation disease UNIPROT Mutations in DSTYK and dominant urinary tract malformations. 23862974 2013
CUI: C1835826
Disease: Renal Hypodysplasia, Nonsyndromic, 1
Renal Hypodysplasia, Nonsyndromic, 1 		0.700 Biomarker disease CTD_human
CUI: C1835826
Disease: Renal Hypodysplasia, Nonsyndromic, 1
Renal Hypodysplasia, Nonsyndromic, 1 		0.700 CausalMutation disease CLINVAR