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: C0149779
Disease: Somatization
Somatization 		21 0 1 4.8E-02 0 0
CUI: C0027443
Disease: Natal Teeth
Natal Teeth 		22 0 1 4.5E-02 0 0
CUI: C0274294
Disease: Chronic mountain sickness
Chronic mountain sickness 		24 0 1 4.2E-02 0 0
CUI: C1832117
Disease: Short humerus
Short humerus 		24 0 1 4.2E-02 0 0
CUI: C1833340
Disease: Synostotic Posterior Plagiocephaly
Synostotic Posterior Plagiocephaly 		25 0 1 4.0E-02 0 0
CUI: C1854928
Disease: Protuberant abdomen
Protuberant abdomen 		25 0 1 4.0E-02 0 0
CUI: C0009451
Disease: Communicating Hydrocephalus
Communicating Hydrocephalus 		26 0 1 3.8E-02 0 0
CUI: C0267834
Disease: Liver cyst
Liver cyst 		26 0 1 3.8E-02 0 0
CUI: C3839753
Disease: Abnormality of nail of toe
Abnormality of nail of toe 		26 0 1 3.8E-02 0 0
CUI: C1860819
Disease: Metopic synostosis
Metopic synostosis 		28 0 1 3.6E-02 0 0
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 1 3.3E-02 0 0
CUI: C0011989
Disease: Camurati-Engelmann Syndrome
Camurati-Engelmann Syndrome 		34 0 1 2.9E-02 0 0
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		34 0 1 2.9E-02 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly 		35 0 1 2.9E-02 0 0
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis 		35 0 1 2.9E-02 0 0
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair 		35 0 1 2.9E-02 0 0
CUI: C0239399
Disease: Short extremities
Short extremities 		38 0 1 2.6E-02 0 0
CUI: C0020256
Disease: Congenital Hydrocephalus
Congenital Hydrocephalus 		39 0 1 2.6E-02 0 0
CUI: C0266039
Disease: Taurodontism
Taurodontism 		40 0 1 2.5E-02 0 0
CUI: C0399352
Disease: Developmental absence of tooth
Developmental absence of tooth 		41 0 1 2.4E-02 0 0
CUI: C1836189
Disease: Radial deviation of finger
Radial deviation of finger 		42 0 1 2.4E-02 0 0
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly 		43 0 1 2.3E-02 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 2.1E-02 0 0
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		52 0 1 1.9E-02 0 0
CUI: C1853737
Disease: Prominent occiput
Prominent occiput 		53 0 1 1.9E-02 0 0