Source: BEFREE ×
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: C4082304
Disease: Oligodontia
Oligodontia 		27 19 5 0.15 1 4.3E-02
CUI: C0266039
Disease: Taurodontism
Taurodontism 		8 1 2 0.12 1 0.20
CUI: C0521648
Disease: Neonatal respiratory failure
Neonatal respiratory failure 		8 0 2 0.12 0 0
CUI: C0040427
Disease: Tooth Abnormalities
Tooth Abnormalities 		9 0 2 0.11 0 0
CUI: C0020608
Disease: Hypodontia
Hypodontia 		55 35 6 1.0E-01 2 5.3E-02
CUI: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 9.1E-02 0 0
CUI: C0206554
Disease: Odontodysplasia
Odontodysplasia 		1 0 1 9.1E-02 0 0
CUI: C0271086
Disease: Toxic maculopathy
Toxic maculopathy 		1 0 1 9.1E-02 0 0
CUI: C0432233
Disease: Trichorhinophalangeal dysplasia type I
Trichorhinophalangeal dysplasia type I 		1 0 1 9.1E-02 0 0
CUI: C0796093
Disease: Odontoonychodermal dysplasia
Odontoonychodermal dysplasia 		1 0 1 9.1E-02 0 0
CUI: C1274743
Disease: Hyperhidrosis Palmaris Et Plantaris
Hyperhidrosis Palmaris Et Plantaris 		1 0 1 9.1E-02 0 0
CUI: C1275074
Disease: Odonto-onycho-dermal dysplasia
Odonto-onycho-dermal dysplasia 		1 1 1 9.1E-02 1 0.20
CUI: C1290511
Disease: Anodontia of Permanent Dentition
Anodontia of Permanent Dentition 		1 0 1 9.1E-02 0 0
CUI: C1833693
Disease: Otodental Dysplasia
Otodental Dysplasia 		1 0 1 9.1E-02 0 0
CUI: C1834013
Disease: Odontoma dysphagia syndrome
Odontoma dysphagia syndrome 		1 0 1 9.1E-02 0 0
CUI: C1835492
Disease: TOOTH AGENESIS, SELECTIVE, 4 (disorder)
TOOTH AGENESIS, SELECTIVE, 4 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C1837341
Disease: Transposition of the Great Arteries, Dextro-Looped 1
Transposition of the Great Arteries, Dextro-Looped 1 		1 0 1 9.1E-02 0 0
CUI: C1857069
Disease: SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder)
SCHOPF-SCHULZ-PASSARGE SYNDROME (disorder) 		1 0 1 9.1E-02 0 0
CUI: C1971810
Disease: Congenital cardiovascular disorder
Congenital cardiovascular disorder 		1 0 1 9.1E-02 0 0
CUI: C2674737
Disease: Abnormality of finger
Abnormality of finger 		1 0 1 9.1E-02 0 0
CUI: C3531771
Disease: Dextrotransposition of the great arteries
Dextrotransposition of the great arteries 		1 0 1 9.1E-02 0 0
CUI: C4025700
Disease: Trichodysplasia
Trichodysplasia 		1 0 1 9.1E-02 0 0
CUI: C4733128
Disease: familial chordoma
familial chordoma 		1 0 1 9.1E-02 0 0
CUI: C0025988
Disease: Microglossia
Microglossia 		2 0 1 8.3E-02 0 0
CUI: C0266604
Disease: Congenital aplasia of inner ear
Congenital aplasia of inner ear 		2 0 1 8.3E-02 0 0