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: C0022904
Disease: Lacrimal Apparatus Diseases
Lacrimal Apparatus Diseases 		1 0 1 1.0E-01 0 0
CUI: C0040947
Disease: Trichostrongyloidiasis
Trichostrongyloidiasis 		1 0 1 1.0E-01 0 0
CUI: C0206554
Disease: Odontodysplasia
Odontodysplasia 		1 0 1 1.0E-01 0 0
CUI: C0406716
Disease: Hypodontia and nail dysgenesis
Hypodontia and nail dysgenesis 		1 0 1 1.0E-01 0 0
CUI: C0495617
Disease: Congenital scoliosis due to bony malformation
Congenital scoliosis due to bony malformation 		1 0 1 1.0E-01 0 0
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		1 15 1 1.0E-01 1 3.7E-02
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		1 0 1 1.0E-01 0 0
CUI: C1334180
Disease: Inflammatory malignant fibrous histiocytoma
Inflammatory malignant fibrous histiocytoma 		1 0 1 1.0E-01 0 0
CUI: C1704335
Disease: Apocrine cystadenoma
Apocrine cystadenoma 		1 0 1 1.0E-01 0 0
CUI: C1832594
Disease: Verloes Bourguignon syndrome
Verloes Bourguignon syndrome 		1 0 1 1.0E-01 0 0
CUI: C1835492
Disease: TOOTH AGENESIS, SELECTIVE, 4 (disorder)
TOOTH AGENESIS, SELECTIVE, 4 (disorder) 		1 24 1 1.0E-01 1 2.8E-02
CUI: C1835493
Disease: Succedaneous Teeth, Agenesis Of
Succedaneous Teeth, Agenesis Of 		1 0 1 1.0E-01 0 0
CUI: C1837750
Disease: Oligodontia-Colorectal Cancer Syndrome
Oligodontia-Colorectal Cancer Syndrome 		1 0 1 1.0E-01 0 0
CUI: C1857069
Disease: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1865092
Disease: TOOTH AGENESIS, SELECTIVE, 2 (disorder)
TOOTH AGENESIS, SELECTIVE, 2 (disorder) 		1 0 1 1.0E-01 0 0
CUI: C1866077
Disease: MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5
MALIGNANT HYPERTHERMIA, SUSCEPTIBILITY TO, 5 		1 0 1 1.0E-01 0 0
CUI: C1970027
Disease: Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility
Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility 		1 0 1 1.0E-01 0 0
CUI: C1970291
Disease: Tooth Agenesis, Selective, 3
Tooth Agenesis, Selective, 3 		1 0 1 1.0E-01 0 0
CUI: C2749982
Disease: THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1
THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 		1 0 1 1.0E-01 0 0
CUI: C2751297
Disease: Tooth Agenesis, Selective, 6
Tooth Agenesis, Selective, 6 		1 0 1 1.0E-01 0 0
CUI: C2910327
Disease: Hemivertebra fusion or failure of segmentation with scoliosis
Hemivertebra fusion or failure of segmentation with scoliosis 		1 0 1 1.0E-01 0 0
CUI: C2930984
Disease: Malignant hyperthermia susceptibility type 5
Malignant hyperthermia susceptibility type 5 		1 0 1 1.0E-01 0 0
CUI: C3150923
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES 		1 0 1 1.0E-01 0 0
CUI: C3554113
Disease: Thin toenail
Thin toenail 		1 0 1 1.0E-01 0 0
CUI: C4013764
Disease: MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES
MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES 		1 0 1 1.0E-01 0 0