Source: INFERRED ×
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: C0001080
Disease: Achondroplasia
Achondroplasia 		1 0 1 1.8E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 0 1 1.8E-02 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis 		1 0 1 1.8E-02 0 0
CUI: C0020039
Disease: Hostility
Hostility 		1 0 1 1.8E-02 0 0
CUI: C0023003
Disease: Langer-Giedion Syndrome
Langer-Giedion Syndrome 		1 2 1 1.8E-02 1 0.20
CUI: C0033141
Disease: Cardiomyopathies, Primary
Cardiomyopathies, Primary 		1 0 1 1.8E-02 0 0
CUI: C0085417
Disease: Epilepsy, Complex Partial
Epilepsy, Complex Partial 		1 0 1 1.8E-02 0 0
CUI: C0158667
Disease: Aplasia of Lacrimal and Salivary Glands
Aplasia of Lacrimal and Salivary Glands 		1 0 1 1.8E-02 0 0
CUI: C0220769
Disease: FG syndrome
FG syndrome 		1 0 1 1.8E-02 0 0
CUI: C0239846
Disease: Hand-wringing
Hand-wringing 		1 0 1 1.8E-02 0 0
CUI: C0265252
Disease: Coffin-Lowry syndrome
Coffin-Lowry syndrome 		1 0 1 1.8E-02 0 0
CUI: C0265338
Disease: Coffin-Siris syndrome
Coffin-Siris syndrome 		1 0 1 1.8E-02 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant 		1 0 1 1.8E-02 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		1 0 1 1.8E-02 0 0
CUI: C0343114
Disease: Woolly hair nevus
Woolly hair nevus 		1 0 1 1.8E-02 0 0
CUI: C0349450
Disease: Soiling
Soiling 		1 0 1 1.8E-02 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		1 0 1 1.8E-02 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing 		1 0 1 1.8E-02 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 1 1 1.8E-02 1 0.25
CUI: C0432233
Disease: Trichorhinophalangeal dysplasia type I
Trichorhinophalangeal dysplasia type I 		1 43 1 1.8E-02 1 2.2E-02
CUI: C0544862
Disease: Neurocutaneous melanosis
Neurocutaneous melanosis 		1 0 1 1.8E-02 0 0
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder) 		1 0 1 1.8E-02 0 0
CUI: C0685678
Disease: Incomplete ossification of pubis
Incomplete ossification of pubis 		1 0 1 1.8E-02 0 0
CUI: C0795888
Disease: AUTISM, SUSCEPTIBILITY TO, X-LINKED 4
AUTISM, SUSCEPTIBILITY TO, X-LINKED 4 		1 0 1 1.8E-02 0 0
CUI: C0796022
Disease: Lujan Fryns syndrome
Lujan Fryns syndrome 		1 0 1 1.8E-02 0 0