3.1.3.56	Oculocerebrorenal Syndrome	https://pubmed.ncbi.nlm.nih.gov/23692838/	A novel OCRL1 gene mutation in a Turkish child with Lowe syndrome.	unassigned	-	
3.1.3.56	Oculocerebrorenal Syndrome	https://pubmed.ncbi.nlm.nih.gov/24614960/	A Novel OCRL1 Mutation in a Patient with the Mild Phenotype of Lowe Syndrome.	causal interaction	4	
3.1.3.56	Oculocerebrorenal Syndrome	https://pubmed.ncbi.nlm.nih.gov/24614960/	A Novel OCRL1 Mutation in a Patient with the Mild Phenotype of Lowe Syndrome.	unassigned	-	
3.1.3.56	Cataract	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	causal interaction	4	
3.1.3.56	Cataract	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	therapeutic application	1	
3.1.3.56	Cataract	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	unassigned	-	
3.1.3.56	Intellectual Disability	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	causal interaction	4	
3.1.3.56	Intellectual Disability	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	therapeutic application	1	
3.1.3.56	Intellectual Disability	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	unassigned	-	
3.1.3.56	Muscular Dystrophies	https://pubmed.ncbi.nlm.nih.gov/33193651/	A Recurrent Pathogenic Variant of INPP5K Underlies Autosomal Recessive Congenital Muscular Dystrophy With Cataracts and Intellectual Disability: Evidence for a Founder Effect in Southern Italy.	causal interaction	4