3.1.3.56	Alzheimer Disease	https://pubmed.ncbi.nlm.nih.gov/27750211/	INPP5D rs35349669 polymorphism with late-onset Alzheimer's disease: A replication study and meta-analysis.	causal interaction	4	
3.1.3.56	Ataxia	https://pubmed.ncbi.nlm.nih.gov/26051944/	Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice.	causal interaction	2	
3.1.3.56	Ataxia	https://pubmed.ncbi.nlm.nih.gov/33792664/	INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH.	causal interaction	4	
3.1.3.56	Carcinoma	https://pubmed.ncbi.nlm.nih.gov/31437542/	Prognostic Value of Inositol Polyphosphate-5-Phosphatase Expression in Recurrent and Metastatic Cutaneous Squamous Cell Carcinoma.	causal interaction	4	
3.1.3.56	Carcinoma, Squamous Cell	https://pubmed.ncbi.nlm.nih.gov/31437542/	Prognostic Value of Inositol Polyphosphate-5-Phosphatase Expression in Recurrent and Metastatic Cutaneous Squamous Cell Carcinoma.	causal interaction	4	
3.1.3.56	Cardiomegaly	https://pubmed.ncbi.nlm.nih.gov/19875726/	Inpp5f Is a Polyphosphoinositide Phosphatase That Regulates Cardiac Hypertrophic Responsiveness.	causal interaction	3	
3.1.3.56	Cataract	https://pubmed.ncbi.nlm.nih.gov/28190456/	Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment.	causal interaction	4	
3.1.3.56	Cataract	https://pubmed.ncbi.nlm.nih.gov/28940338/	INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family.	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.	causal interaction	4	
3.1.3.56	Cataract	https://pubmed.ncbi.nlm.nih.gov/28190459/	Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy.	causal interaction	3