FIGNL1, fidgetin like 1, 63979

N. diseases: 23; N. variants: 60
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0022665
Disease: Kidney Neoplasm
Kidney Neoplasm 		0.300 Biomarker disease CTD_human Investigation of the early-response genes in chemical-induced renal carcinogenicity for the prediction of chemical carcinogenicity in rats. 28321044 2017
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		0.300 Biomarker disease CTD_human Investigation of the early-response genes in chemical-induced renal carcinogenicity for the prediction of chemical carcinogenicity in rats. 28321044 2017
CUI: C1305855
Disease: Body mass index
Body mass index 		0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.100 GeneticVariation disease GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250 2013
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.100 GeneticVariation disease GWASCAT Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. 22076464 2012
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.100 GeneticVariation phenotype GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
CUI: C1291564
Disease: Deficiency of aromatic-L-amino-acid decarboxylase
Deficiency of aromatic-L-amino-acid decarboxylase 		0.100 CausalMutation disease CLINVAR Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. 20505134 2010
CUI: C1291564
Disease: Deficiency of aromatic-L-amino-acid decarboxylase
Deficiency of aromatic-L-amino-acid decarboxylase 		0.100 GeneticVariation disease CLINVAR Clinical and biochemical features of aromatic L-amino acid decarboxylase deficiency. 20505134 2010
CUI: C1961102
Disease: Precursor Cell Lymphoblastic Leukemia Lymphoma
Precursor Cell Lymphoblastic Leukemia Lymphoma 		0.100 GeneticVariation disease GWASDB Germline genomic variants associated with childhood acute lymphoblastic leukemia. 19684603 2009
CUI: C1291564
Disease: Deficiency of aromatic-L-amino-acid decarboxylase
Deficiency of aromatic-L-amino-acid decarboxylase 		0.100 CausalMutation disease CLINVAR Aromatic L-amino acid decarboxylase enzyme activity in deficient patients and heterozygotes. 17240182 2007
CUI: C1291564
Disease: Deficiency of aromatic-L-amino-acid decarboxylase
Deficiency of aromatic-L-amino-acid decarboxylase 		0.100 GeneticVariation disease CLINVAR Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
CUI: C1291564
Disease: Deficiency of aromatic-L-amino-acid decarboxylase
Deficiency of aromatic-L-amino-acid decarboxylase 		0.100 CausalMutation disease CLINVAR Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. 15079002 2004
CUI: C0011991
Disease: Diarrhea
Diarrhea 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0013362
Disease: Dysarthria
Dysarthria 		0.100 GeneticVariation disease CLINVAR
CUI: C0020649
Disease: Hypotension
Hypotension 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		0.100 GeneticVariation disease CLINVAR
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0086439
Disease: Hypokinesia
Hypokinesia 		0.100 GeneticVariation phenotype CLINVAR
CUI: C0424503
Disease: Dysmorphic facies
Dysmorphic facies 		0.100 GeneticVariation phenotype CLINVAR
CUI: C1836996
Disease: Disproportionate tall stature
Disproportionate tall stature 		0.100 GeneticVariation phenotype CLINVAR
CUI: C1837639
Disease: Intermittent hypothermia
Intermittent hypothermia 		0.100 GeneticVariation phenotype CLINVAR
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		0.100 GeneticVariation phenotype CLINVAR
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		0.100 GeneticVariation phenotype CLINVAR
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		0.100 GeneticVariation phenotype CLINVAR
CUI: C2700617
Disease: Irritation - emotion
Irritation - emotion 		0.100 GeneticVariation phenotype CLINVAR