Disease #00003 (ALS (Amyotrophic Lateral Sclerosis), OMIM:105400)
Official abbreviation |
ALS |
Name |
Amyotrophic Lateral Sclerosis |
OMIM ID |
105400 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1029 |
Phenotype entries for this disease |
508 |
Associated with 54 genes |
ALS2, ANG, ANXA11, APEX1, ARHGEF28, C9orf72, CCNF, CHCHD10, CHGB, CHMP2B, CYLD, DCTN1, DNAJC7, DPYSL3, ERLIN1, FUS, GLE1, GRN, HFE, HNRNPA1, 34 more...ALS2, ANG, ANXA11, APEX1, ARHGEF28, C9orf72, CCNF, CHCHD10, CHGB, CHMP2B, CYLD, DCTN1, DNAJC7, DPYSL3, ERLIN1, FUS, GLE1, GRN, HFE, HNRNPA1, KIF5A, KIFAP3, LIF, LRSAM1, MATR3, NEK1, NOTCH3, OGG1, OPTN, PARK7, PFN1, PON1, PON2, PON3, PRPH, SETX, SIGMAR1, SOD1, SORD, SPAST, SPG11, SPTLC1, SPTLC2, SQSTM1, SS18L1, TARDBP, TBK1, TRPM7, TUBA4A, TYROBP, UBQLN2, UNC13A, VAPB, VCP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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