IHH, Indian hedgehog signaling molecule, 3549

N. diseases: 130; N. variants: 14
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
0.010 Biomarker disease BEFREE In contrast, IHH was almost lost in both colorectal adenomas and CRCs. 20854074 2010
CUI: C1608408
Disease: Malignant transformation
Malignant transformation
0.010 AlteredExpression phenotype BEFREE The isolated IHH cDNA had no sequence alterations, suggesting that upregulation of IHH expression may contribute to malignant transformation. 19793350 2010
CUI: C0035344
Disease: Retinopathy of Prematurity
Retinopathy of Prematurity
0.010 Biomarker disease BEFREE Extending this analysis to include genotyping data from a larger genetic study of prematurity (455 SNPs in 153 genes), we found SNPs in five genes associated with the development of ROP: IHH (p = 0.003), AGTR1 (p = 0.005), TBX5 (p = 0.003), CETP (p = 0.004), and GP1BA (p = 0.005). 18787502 2009
CUI: C0005940
Disease: Bone Diseases
Bone Diseases
0.010 Biomarker group LHGDN Runx2 transcriptional activation of Indian Hedgehog and a downstream bone metastatic pathway in breast cancer cells. 18829534 2008
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.010 Biomarker phenotype LHGDN Runx2 transcriptional activation of Indian Hedgehog and a downstream bone metastatic pathway in breast cancer cells. 18829534 2008
CUI: C0008479
Disease: Chondrosarcoma
Chondrosarcoma
0.010 AlteredExpression disease LHGDN Differential expression of runx2 and Indian hedgehog in cartilaginous tumors. 17387386 2007
CUI: C0206637
Disease: Mesenchymal Chondrosarcoma
Mesenchymal Chondrosarcoma
0.010 AlteredExpression disease LHGDN Differential expression of runx2 and Indian hedgehog in cartilaginous tumors. 17387386 2007
CUI: C0029423
Disease: Cartilaginous exostosis
Cartilaginous exostosis
0.010 AlteredExpression disease BEFREE The expression patterns of IHH (Indian hedgehog) and FGFR3 (Fibroblast Growth Factor Receptor 3) were similar with transcripts expressed throughout osteochondromas. 16476576 2006
CUI: C0410530
Disease: Metachondromatosis
Metachondromatosis
0.010 AlteredExpression disease BEFREE IHH/PTHLH signalling molecules were expressed in DEH and MC as shown by both qPCR and immunohistochemistry, suggesting that this pathway is active. 16622899 2006
CUI: C0432282
Disease: Dysplasia epiphysealis hemimelica
Dysplasia epiphysealis hemimelica
0.010 AlteredExpression disease BEFREE IHH/PTHLH signalling molecules were expressed in DEH and MC as shown by both qPCR and immunohistochemistry, suggesting that this pathway is active. 16622899 2006
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 AlteredExpression disease BEFREE SHH up-regulation, IHH upregulation and HHIP down-regulation lead to aberrant activation of Hedgehog signaling through PTCH1 to GLI1 in gastric cancer. 16258256 2005
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 AlteredExpression disease BEFREE SHH up-regulation, IHH upregulation and HHIP down-regulation lead to aberrant activation of Hedgehog signaling through PTCH1 to GLI1 in gastric cancer. 16258256 2005
CUI: C0030297
Disease: Pancreatic Neoplasm
Pancreatic Neoplasm
0.010 AlteredExpression disease LHGDN Indian hedgehog signaling pathway: expression and regulation in pancreatic cancer. 15146555 2004
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.020 AlteredExpression disease BEFREE A total of 38 patients with PTC were included and the normal thyroid follicular epithelial cell line Nthy‑ori 3‑1 and PTC cell line IHH‑4 were also used. 30720110 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 AlteredExpression group BEFREE The percentage of positive WIF-1 protein expression was significantly higher, while positive Ihh protein expression was significantly lower in patients with well-differentiated lung squamous cell carcinoma and adenocarcinoma, tumor node metastasis (TNM) stage I disease, and lymph node metastasis than that in patients with poorly differentiated tumor, TNM stage III disease, and lymph node metastasis (P<0.05, <0.01). 27801732 2018
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 Biomarker disease BEFREE The present investigation examines the capacity of co-cultures between the HCEC colon epithelial cells and the HCT-116 colorectal cancer cells (mimicking the primary site of tumour growth) and between IHH hepatocytes and the HCT-116 colorectal cancer cells (metastatic site) to influence the effects of NAMI-A (imidazolium trans-imidazoledimethylsulphoxidetetrachloro ruthenate) on the tumour cells themselves. 28064102 2017
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.020 Biomarker group BEFREE The present investigation examines the capacity of co-cultures between the HCEC colon epithelial cells and the HCT-116 colorectal cancer cells (mimicking the primary site of tumour growth) and between IHH hepatocytes and the HCT-116 colorectal cancer cells (metastatic site) to influence the effects of NAMI-A (imidazolium trans-imidazoledimethylsulphoxidetetrachloro ruthenate) on the tumour cells themselves. 28064102 2017
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma
0.020 Biomarker disease BEFREE And, NONHSAT037832 was also significantly downregulated in two PTC cell lines (K1 and IHH-4) compared to normal thyroid follicular epithelial cell line Nthy-ori 3-1 (P < 0.01). 26611646 2016
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.020 AlteredExpression disease BEFREE The culture medium conditioned by the IHH hepatic cell line, and the extracellular matrix (ECM) proteins, modulate the activation of α5β1 integrin in the colon cancer cell line HCT-116, and drives FAK phosphorylation during the process of cell adhesion to fibronectin, one of the main components of liver ECM. 25857463 2015
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.020 AlteredExpression disease BEFREE The culture medium conditioned by the IHH hepatic cell line, and the extracellular matrix (ECM) proteins, modulate the activation of α5β1 integrin in the colon cancer cell line HCT-116, and drives FAK phosphorylation during the process of cell adhesion to fibronectin, one of the main components of liver ECM. 25857463 2015
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
0.020 GeneticVariation disease BEFREE We report a female with combined pituitary hormone deficiencies (GH, TSH, gonadotropin and ACTH), except for prolactin, as a consequence of PROP1 mutation, and a male with KS (anosmia and IHH) due to Kal 2 gene (fibroblast growth factor receptor 1- FGFR1) mutation, both of whom in adulthood presented with prolactinomas. 22801565 2013
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
0.020 PosttranslationalModification disease BEFREE Methylation analysis revealed that IHH promoter was hypermethylated in colon cancer cell lines. 19856079 2010
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 PosttranslationalModification disease BEFREE IHH promoter methylation was frequently observed in colorectal adenomas (55.2%, p = 0.004) and CRCs (70.6%, p<0.001) compared with that in hyperplastic polyps (11.8%). 20854074 2010
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
0.020 PosttranslationalModification disease BEFREE Methylation analysis revealed that IHH promoter was hypermethylated in colon cancer cell lines. 19856079 2010
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome
0.020 GeneticVariation disease BEFREE One hundred IHH probands (50 nIHH and 50 KS) with no known mutations were examined for mutations in the PROK2 gene. 17959774 2007