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Chemical Aluminum

These diseases are associated with Aluminum or its descendants. Each association is curated (M marker/mechanism and/or T therapeutic) and/or inferred (via a curated gene interaction).

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101–150 of 1,241 results.
  Chemical Disease Direct Evidence Enrichment Analysis Inference Network Inference Score References
101. Aluminum Cleft palate X-linked     1 gene: TBX22 5.95 1
102. Aluminum NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A     1 gene: NYX 5.95 1
103. Aluminum Retinitis Pigmentosa 30     1 gene: FSCN2 5.95 1
104. Aluminum Breast Neoplasms  
42 genes: AFP | AR | ARHGDIA | BAX | BCL2A1 | C10ORF10 | CDH1 | CLUL1 | COL7A1 | CUL5 | EPOR | ESR1 | FOXP3 | GPX1 | HEYL | HMOX1 | HNRNPR | HOXD11 | IGF1 | IL1B | JUN | KIT | MAL | MMP2 | MMP9 | MTR | NOS2 | PGR | PLA2G4A | PTGS2 | PTHLH | RAD51B | RIBC2 | SFRP5 | SIM1 | SLC2A1 | SNAI1 | SOD2 | TFRC | TNF | TNFSF10 | WWOX 		5.94 51
105. Aluminum Allanson Pantzar McLeod syndrome  
2 genes: ACE | AGTR1 		5.92 1
106. Aluminum RENAL TUBULAR DYSGENESIS  
2 genes: ACE | AGTR1 		5.92 2
107. Aluminum Down Syndrome  
4 genes: GATA1 | MTR | S100B | SLC19A1 		5.86 4
108. Aluminum Vipoma  
2 genes: IFNA1 | MEN1 		5.85 1
109. Aluminum Fatigue     1 gene: IFNA2 5.83 1
110. Aluminum Weight Loss  
2 genes: ADIPOQ | IFNA2 		5.82 2
111. Aluminum Carotid Artery Diseases  
4 genes: CD163 | FASLG | HMOX1 | MRAS 		5.81 3
112. Aluminum Hypotension  
14 genes: ACE | ALB | BDKRB2 | CAT | CTF1 | DRD1A | DRD2 | HRH1 | HTR1B | HTR1D | IL1B | IL2 | LTF | TNF 		5.81 18
113. Aluminum Retinitis pigmentosa 1     1 gene: RP1 5.80 1
114. Aluminum SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE     1 gene: HES7 5.80 1
115. Aluminum Eye Diseases, Hereditary  
2 genes: LRAT | RLBP1 		5.70 1
116. Aluminum Acute Kidney Injury  
10 genes: ALB | AMBP | BAX | G6PD | HAVCR1 | HMOX1 | IFNA2 | KLK1 | MPO | TNF 		5.69 16
117. Aluminum Usher Syndrome, Type IG     1 gene: USH1G 5.69 1
118. Aluminum Carcinoma, squamous cell of head and neck  
5 genes: HOXA5 | HOXD11 | KISS1 | PTGS2 | SOD2 		5.67 4
119. Aluminum Coffin-Siris syndrome  
2 genes: ARID1B | SMARCA2 		5.65 2
120. Aluminum Drug Toxicity  
10 genes: HAVCR1 | HMOX1 | HTR2B | IGF1 | IL3 | MTR | NAT1 | PTGS2 | SLC19A1 | SLC34A2 		5.65 10
121. Aluminum Carcinoma, Intraductal, Noninfiltrating  
2 genes: HIF1A | SLC2A1 		5.64 1
122. Aluminum Muscle Weakness     1 gene: AMPD1 5.63 1
123. Aluminum Pulmonary Fibrosis  
11 genes: ELN | HMOX1 | IGF1 | IL13 | IL1B | IL4 | IL5 | MMP2 | MMP9 | PTX3 | TNF 		5.61 11
124. Aluminum Lamellar ichthyosis, type 3     1 gene: CYP4F22 5.60 1
125. Aluminum Pruritus  
2 genes: HRH1 | HRH4 		5.60 1
126. fluoroaluminum Lewy Body Disease     1 gene: IGF2 5.56 1
127. Aluminum Congenital Disorder Of Glycosylation, Type In     1 gene: RFT1 5.53 1
128. Aluminum NYSTAGMUS 6, CONGENITAL, X-LINKED     1 gene: GPR143 5.53 1
129. Aluminum Ocular Albinism type 1     1 gene: GPR143 5.53 1
130. Aluminum Abdominal Pain     1 gene: IFNA2 5.49 1
131. Aluminum Arthritis, Experimental  
8 genes: ACSL4 | CAT | COL2A1 | IL13 | IL1B | IL4 | MPO | TNF 		5.48 8
132. Aluminum Long QT Syndrome     1 gene: SCN5A 5.48 8
133. Aluminum Charcot-Marie-Tooth disease, Type 4C     1 gene: SH3TC2 5.47 1
134. Aluminum Ectodermal Dysplasia 1, Anhidrotic     1 gene: EDA 5.47 1
135. Aluminum MONONEUROPATHY OF THE MEDIAN NERVE, MILD     1 gene: SH3TC2 5.47 1
136. Aluminum Retinal Cone Dystrophy 3A     1 gene: PDE6H 5.47 1
137. Aluminum Tooth Agenesis, Selective, X-Linked, 1     1 gene: EDA 5.47 1
138. Aluminum Hypertension, Essential  
4 genes: AGTR1 | ECE1 | NOS2 | PTGIS 		5.46 1
139. Aluminum Amnesia  
3 genes: APP | GNAI1 | IL2 		5.42 3
140. Aluminum Cornea Plana 2     1 gene: KERA 5.41 1
141. Aluminum N-acetyl glutamate synthetase deficiency     1 gene: NAGS 5.41 3
142. fluoroaluminum Wilms Tumor     1 gene: IGF2 5.40 1
143. Aluminum Torsades de Pointes     1 gene: SCN5A 5.39 2
144. Aluminum Rickets  
3 genes: PTH | PTH1R | VDR 		5.38 3
145. Aluminum Carney Complex Variant     1 gene: MYH8 5.37 1
146. Aluminum Elliptocytosis 1     1 gene: EPB41 5.37 1
147. Aluminum Hecht syndrome     1 gene: MYH8 5.37 1
148. Aluminum Hydrolethalus syndrome     1 gene: KIF7 5.37 1
149. Aluminum Arthrogryposis renal dysfunction cholestasis syndrome     1 gene: VIPAS39 5.36 2
150. Aluminum Cataract, Congenital Zonular, with Sutural Opacities     1 gene: CRYBA1 5.32 1
101–150 of 1,241 results.
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