Synonyms: AIFM1 apoptosis-inducing factor, mitochondria-associated, 1 programmed cell death 8 apoptosis-inducing factor
Term information
http://www.ncbi.nlm.nih.gov/pubmed/28967629
http://www.ncbi.nlm.nih.gov/pubmed/12114629
http://www.ncbi.nlm.nih.gov/pubmed/25986071
http://www.ncbi.nlm.nih.gov/pubmed/12446902
http://www.ncbi.nlm.nih.gov/pubmed/23217327
http://www.ncbi.nlm.nih.gov/pubmed/3856385
http://www.ncbi.nlm.nih.gov/pubmed/22019070
http://www.ncbi.nlm.nih.gov/pubmed/31523922
http://www.ncbi.nlm.nih.gov/pubmed/26173962
http://www.ncbi.nlm.nih.gov/pubmed/25583628
http://www.ncbi.nlm.nih.gov/pubmed/17088543
http://www.ncbi.nlm.nih.gov/pubmed/16816020
http://www.ncbi.nlm.nih.gov/pubmed/23239615
http://www.ncbi.nlm.nih.gov/pubmed/11279485
http://www.ncbi.nlm.nih.gov/pubmed/25934856
http://www.ncbi.nlm.nih.gov/pubmed/19723031
http://www.ncbi.nlm.nih.gov/pubmed/16924009
http://www.ncbi.nlm.nih.gov/pubmed/17116882
http://www.ncbi.nlm.nih.gov/pubmed/28842795
http://www.ncbi.nlm.nih.gov/pubmed/10486082
http://www.ncbi.nlm.nih.gov/pubmed/16788063
http://www.ncbi.nlm.nih.gov/pubmed/12353028
http://www.ncbi.nlm.nih.gov/pubmed/9989411
http://www.ncbi.nlm.nih.gov/pubmed/20362274
http://www.ncbi.nlm.nih.gov/pubmed/27102849
http://www.ncbi.nlm.nih.gov/pubmed/17116881
https://identifiers.org/hgnc/8768
http://linkedlifedata.com/resource/umls/id/C0795910
http://linkedlifedata.com/resource/umls/id/C1846148
http://linkedlifedata.com/resource/umls/id/C5231520
https://www.genenames.org/data/gene-symbol-report/#!/hgnc_id/AIFM1
http://linkedlifedata.com/resource/umls/id/C3151753
https://www.ncbi.nlm.nih.gov/gene/9131
http://linkedlifedata.com/resource/umls/id/C1845095
http://linkedlifedata.com/resource/umls/id/C1826618
Term relations
- SO_0000704
- RO_0003302 some spondyloepimetaphyseal dysplasia, x-linked, with hypomyelinating leukodystrophy
- RO_0003302 some combined oxidative phosphorylation deficiency 6
- RO_0002525 some CHR_9606chrXq26.1
- RO_0003302 some charcot-marie-tooth disease, X-linked recessive, 4, with or without cerebellar ataxia
- RO_0003302 some deafness, X-linked 5, with peripheral neuropathy