Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0234144
Disease: Dysgraphia
Dysgraphia 		43 0 19 0.14 0 0
CUI: C0016689
Disease: Freckles
Freckles 		45 0 18 0.13 0 0
CUI: C0234132
Disease: Pyramidal sign
Pyramidal sign 		155 0 28 0.12 0 0
CUI: C0085632
Disease: Apathy
Apathy 		83 0 19 0.11 0 0
CUI: C0751706
Disease: Primary Progressive Nonfluent Aphasia
Primary Progressive Nonfluent Aphasia 		21 0 13 0.10 0 0
CUI: C0003635
Disease: Apraxias
Apraxias 		71 0 17 1.0E-01 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 0 35 9.9E-02 0 0
CUI: C2314896
Disease: Familial Atypical Mole Melanoma Syndrome
Familial Atypical Mole Melanoma Syndrome 		30 0 13 9.8E-02 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 12 9.7E-02 0 0
CUI: C0240735
Disease: Personality Change
Personality Change 		43 0 14 9.7E-02 0 0
CUI: C0221271
Disease: Elastosis perforans serpiginosa
Elastosis perforans serpiginosa 		66 4 16 9.6E-02 1 1.0E-01
CUI: C1865412
Disease: Abnormal lower motor neuron morphology
Abnormal lower motor neuron morphology 		23 0 12 9.4E-02 0 0
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
Behavioral variant of frontotemporal dementia 		35 0 13 9.4E-02 0 0
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE 		108 0 19 9.3E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		487 0 51 9.2E-02 0 0
CUI: C4021976
Disease: Abnormality of the lymphatic system
Abnormality of the lymphatic system 		16 0 11 9.1E-02 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		477 0 49 9.0E-02 0 0
CUI: C0026838
Disease: Muscle Spasticity
Muscle Spasticity 		580 0 57 8.9E-02 0 0
CUI: C0242422
Disease: Parkinsonian Disorders
Parkinsonian Disorders 		373 95 40 8.9E-02 1 9.9E-03
CUI: C0424296
Disease: Social disinhibition
Social disinhibition 		56 0 14 8.9E-02 0 0
CUI: C0233401
Disease: Psychiatric symptom
Psychiatric symptom 		95 0 17 8.8E-02 0 0
CUI: C4551584
Disease: Brain atrophy
Brain atrophy 		182 0 24 8.8E-02 0 0
CUI: C0151908
Disease: Dry skin
Dry skin 		159 0 22 8.7E-02 0 0
CUI: C0151514
Disease: Atrophic condition of skin
Atrophic condition of skin 		111 0 18 8.6E-02 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 11 8.6E-02 0 0