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: C3810090
Disease: L-FERRITIN DEFICIENCY
L-FERRITIN DEFICIENCY 		1 0 1 1.00 0 0
CUI: C4016051
Disease: L-FERRITIN DEFICIENCY, AUTOSOMAL RECESSIVE
L-FERRITIN DEFICIENCY, AUTOSOMAL RECESSIVE 		1 0 1 1.00 0 0
CUI: C4024952
Disease: Cavitation of the basal ganglia
Cavitation of the basal ganglia 		1 0 1 1.00 0 0
CUI: C0241012
Disease: Decreased serum ferritin
Decreased serum ferritin 		3 0 1 0.33 0 0
CUI: C0854279
Disease: Basal ganglion degeneration
Basal ganglion degeneration 		3 0 1 0.33 0 0
CUI: C4024935
Disease: Subcortical dementia
Subcortical dementia 		3 0 1 0.33 0 0
CUI: C1833213
Disease: Hyperferritinemia, hereditary, with congenital cataracts
Hyperferritinemia, hereditary, with congenital cataracts 		10 0 1 1.0E-01 0 0
CUI: C0234517
Disease: Anarthria speech disorder
Anarthria speech disorder 		11 0 1 9.1E-02 0 0
CUI: C0240341
Disease: Micrographia
Micrographia 		14 0 1 7.1E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 0 1 6.7E-02 0 0
CUI: C0158551
Disease: Embryonal nuclear cataract (disorder)
Embryonal nuclear cataract (disorder) 		16 0 1 6.2E-02 0 0
CUI: C0270724
Disease: Infantile Neuroaxonal Dystrophy
Infantile Neuroaxonal Dystrophy 		17 0 1 5.9E-02 0 0
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy 		17 0 1 5.9E-02 0 0
CUI: C1963946
Disease: Laryngeal dystonia
Laryngeal dystonia 		17 0 1 5.9E-02 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 1 5.6E-02 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 1 5.3E-02 0 0
CUI: C0018523
Disease: Hallervorden-Spatz Syndrome
Hallervorden-Spatz Syndrome 		22 0 1 4.5E-02 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 1 4.3E-02 0 0
CUI: C0241013
Disease: Increased serum ferritin
Increased serum ferritin 		23 0 1 4.3E-02 0 0
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia 		26 0 1 3.8E-02 0 0
CUI: C3854388
Disease: Hyperferritinaemia
Hyperferritinaemia 		26 0 1 3.8E-02 0 0
CUI: C4316810
Disease: Writer's Cramp
Writer's Cramp 		26 0 1 3.8E-02 0 0
CUI: C1856963
Disease: Fragile nails
Fragile nails 		27 0 1 3.7E-02 0 0
CUI: C0813217
Disease: Expressionless face
Expressionless face 		31 0 1 3.2E-02 0 0
CUI: C0023882
Disease: Little's Disease
Little's Disease 		37 0 1 2.7E-02 0 0