Source: MGD

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C3280797
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2P 		disease 0.910 strong 1.000 1 0 2010 2019
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		disease 0.680 None 0.875 1 0 2010 2019
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		disease 0.500 None 1.000 1 0 2010 2013
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder) 		disease 0.200 None 1.000 1 0 2013 2013
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		group 0.200 None 1.000 1 0 2013 2013
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		disease 0.200 None 1.000 1 0 2013 2013
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		disease 0.200 None 1.000 1 0 2013 2013
Entrez Id: 90678
Gene Symbol: LRSAM1
LRSAM1 		leucine rich repeat and sterile alpha motif containing 1 0.638 0.500 3.1E-13
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		disease 0.200 None 1.000 1 0 2013 2013