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: C3267076
Disease: Familial scaphocephaly syndrome
Familial scaphocephaly syndrome 		1 0 1 0.33 0 0
CUI: C3552414
Disease: Deviation of the thumb
Deviation of the thumb 		1 0 1 0.33 0 0
CUI: C4016344
Disease: PFEIFFER SYNDROME VARIANT
PFEIFFER SYNDROME VARIANT 		1 0 1 0.33 0 0
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: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 0 2 0.29 0 0
CUI: C0025490
Disease: Mesonephroma
Mesonephroma 		2 0 1 0.25 0 0
CUI: C0234512
Disease: Prosopagnosia
Prosopagnosia 		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: C0795820
Disease: Chromosome 7, trisomy 7p
Chromosome 7, trisomy 7p 		2 0 1 0.25 0 0
CUI: C1450010
Disease: Plagiocephaly, Nonsynostotic
Plagiocephaly, Nonsynostotic 		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 16 1 0.25 1 6.2E-02
CUI: C1863363
Disease: Cartilaginous trachea
Cartilaginous trachea 		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
CUI: C3552574
Disease: HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 6 WITH OR WITHOUT ANOSMIA 		2 0 1 0.25 0 0
CUI: C3872820
Disease: Congenital pulmonary acinar dysplasia
Congenital pulmonary acinar dysplasia 		2 0 1 0.25 0 0