Disease #00002 (AD (Alzheimer Disease), OMIM:104300)
Official abbreviation |
AD |
Name |
Alzheimer Disease |
OMIM ID |
104300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
634 |
Phenotype entries for this disease |
- |
Associated with 69 genes |
ABCA7, AGBL3, APOE, APP, ATP8B3, C16orf96, C3orf20, CASS4, CD2AP, CD33, CELF1, CENPJ, CFAP70, CHGB, CHMP2B, CLU, CR1, CST3, CTSF, EBLN1, 49 more...ABCA7, AGBL3, APOE, APP, ATP8B3, C16orf96, C3orf20, CASS4, CD2AP, CD33, CELF1, CENPJ, CFAP70, CHGB, CHMP2B, CLU, CR1, CST3, CTSF, EBLN1, FAM47E, FERMT2, FPR1, FRAS1, GAL3ST4, GPR45, HERC6, HFE, HMGCR, INPP5D, IP6K3, KLHDC4, MAGI3, MAPT, MS4A1, MS4A13, MS4A14, MS4A2, MS4A3, MS4A4A, MS4A4E, MS4A6A, MS4A6E, MS4A7, MYCBPAP, NFATC1, NLGN1, OPRD1, OPRM1, OR52E4, PICALM, PRNP, PSEN1, PSEN2, PTK2B, RGS11, SLC24A4, SORL1, TM2D3, TREM2, TREML1, TREML2, TREML4, TTBK2, TTR, UNC5C, WDR46, ZCWPW1, ZNF646 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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