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: C4016345
Disease: PFEIFFER SYNDROME, TYPE III
PFEIFFER SYNDROME, TYPE III 		1 0 1 0.33 0 0
CUI: C4016346
Disease: CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL
CRANIOSYNOSTOSIS, NONSYNDROMIC UNICORONAL 		1 0 1 0.33 0 0
CUI: C4023454
Disease: Metopic depression
Metopic depression 		1 0 1 0.33 0 0
CUI: C4023628
Disease: Mild fetal ventriculomegaly
Mild fetal ventriculomegaly 		1 0 1 0.33 0 0
CUI: C4023749
Disease: Abnormality of the zygomatic bone
Abnormality of the zygomatic bone 		1 0 1 0.33 0 0
CUI: C4073134
Disease: Abnormality of the periosteum
Abnormality of the periosteum 		1 0 1 0.33 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 0.25 0 0
CUI: C0025490
Disease: Mesonephroma
Mesonephroma 		2 0 1 0.25 0 0
CUI: C0042940
Disease: Voice Disorders
Voice Disorders 		2 0 1 0.25 0 0
CUI: C0221150
Disease: Swallowing painful
Swallowing painful 		2 0 1 0.25 0 0
CUI: C0264306
Disease: Laryngeal Obstruction
Laryngeal Obstruction 		2 0 1 0.25 0 0
CUI: C0432124
Disease: Unicoronal craniosynostosis
Unicoronal craniosynostosis 		2 0 1 0.25 0 0
CUI: C1168153
Disease: Arterial calcification
Arterial calcification 		2 0 1 0.25 0 0
CUI: C1332866
Disease: Adenocarcinoma of cecum
Adenocarcinoma of cecum 		2 0 1 0.25 0 0
CUI: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic 		2 0 1 0.25 0 0
CUI: C1849227
Disease: Cleft of chin
Cleft of chin 		2 0 1 0.25 0 0
CUI: C1851797
Disease: Palmoplantar cutis gyrata
Palmoplantar cutis gyrata 		2 0 1 0.25 0 0
CUI: C1852406
Disease: Cutis Gyrata Syndrome of Beare And Stevenson
Cutis Gyrata Syndrome of Beare And Stevenson 		2 0 1 0.25 0 0
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea 		2 0 1 0.25 0 0
CUI: C1863382
Disease: Absent first metatarsal
Absent first metatarsal 		2 0 1 0.25 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease 		2 0 1 0.25 0 0
CUI: C1863406
Disease: Anomalous tracheal cartilage
Anomalous tracheal cartilage 		2 0 1 0.25 0 0
CUI: C2350233
Disease: Antley-Bixler Syndrome Phenotype
Antley-Bixler Syndrome Phenotype 		2 0 1 0.25 0 0
CUI: C2931888
Disease: Pfeiffer type acrocephalosyndactyly
Pfeiffer type acrocephalosyndactyly 		2 0 1 0.25 0 0
CUI: C3150931
Disease: Steep acetabular roof
Steep acetabular roof 		2 0 1 0.25 0 0