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: C1842466
Disease: Uniparental disomy, paternal, chromosome 14
Uniparental disomy, paternal, chromosome 14 		7 0 3 0.33 0 0
CUI: C1708107
Disease: Functioning Pancreatic Neuroendocrine Tumor
Functioning Pancreatic Neuroendocrine Tumor 		1 0 1 0.20 0 0
CUI: C0340369
Disease: Functional mitral regurgitation
Functional mitral regurgitation 		2 0 1 0.17 0 0
CUI: C4015558
Disease: Temple syndrome
Temple syndrome 		10 0 2 0.15 0 0
CUI: C2349419
Disease: Cluster headaches and other trigeminal autonomic cephalgias
Cluster headaches and other trigeminal autonomic cephalgias 		3 0 1 0.14 0 0
CUI: C4707793
Disease: Isochromosomy Yp
Isochromosomy Yp 		3 0 1 0.14 0 0
CUI: C0795934
Disease: Digitorenocerebral Syndrome
Digitorenocerebral Syndrome 		4 0 1 0.12 0 0
CUI: C0796184
Disease: Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence
Corpus Callosum, Agenesis of, with Facial Anomalies and Robin Sequence 		4 0 1 0.12 0 0
CUI: C1304300
Disease: Skin Nodular Basal Cell Carcinoma
Skin Nodular Basal Cell Carcinoma 		4 0 1 0.12 0 0
CUI: C1377589
Disease: Regressing nevus
Regressing nevus 		4 0 1 0.12 0 0
CUI: C4083056
Disease: Basal cell carcinoma, nodular
Basal cell carcinoma, nodular 		4 0 1 0.12 0 0
CUI: C4023422
Disease: Long palm
Long palm 		5 0 1 0.11 0 0
CUI: C0268615
Disease: 5,10-Methylenetetrahydrofolate reductase deficiency
5,10-Methylenetetrahydrofolate reductase deficiency 		6 0 1 1.0E-01 0 0
CUI: C0038019
Disease: Spondylosis
Spondylosis 		7 0 1 9.1E-02 0 0
CUI: C1857627
Disease: Chorioretinal dystrophy
Chorioretinal dystrophy 		7 0 1 9.1E-02 0 0
CUI: C4551676
Disease: Laryngismus stridulus
Laryngismus stridulus 		7 0 1 9.1E-02 0 0
CUI: C0011998
Disease: Diastema of Teeth
Diastema of Teeth 		9 0 1 7.7E-02 0 0
CUI: C0677608
Disease: Chorioangioma
Chorioangioma 		9 0 1 7.7E-02 0 0
CUI: C0029077
Disease: Ophthalmia, Sympathetic
Ophthalmia, Sympathetic 		11 0 1 6.7E-02 0 0
CUI: C0023472
Disease: Leukemia, Myeloid, Accelerated Phase
Leukemia, Myeloid, Accelerated Phase 		12 0 1 6.2E-02 0 0
CUI: C0278884
Disease: Melanoma recurrent
Melanoma recurrent 		12 0 1 6.2E-02 0 0
CUI: C4281771
Disease: Thin eyebrow
Thin eyebrow 		12 0 1 6.2E-02 0 0
CUI: C1864100
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IB
PSEUDOHYPOPARATHYROIDISM, TYPE IB 		13 0 1 5.9E-02 0 0
CUI: C0206740
Disease: Calcifying Odontogenic Cyst
Calcifying Odontogenic Cyst 		15 0 1 5.3E-02 0 0
CUI: C0026825
Disease: Flaccid Muscle Tone
Flaccid Muscle Tone 		16 0 1 5.0E-02 0 0