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: C0266177
Disease: Megaduodenum
Megaduodenum
1 0 1 0.12 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability
1 0 1 0.12 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects
1 0 1 0.12 0 0
Undifferentiated type acute leukemia
1 0 1 0.12 0 0
Precursor B-lymphoblastic lymphoma stage II
1 0 1 0.12 0 0
CUI: C1336727
Disease: Testicular Sarcoma
Testicular Sarcoma
1 0 1 0.12 0 0
CUI: C1849164
Disease: Long, smooth philtrum
Long, smooth philtrum
1 1 1 0.12 1 3.8E-03
CUI: C1855286
Disease: Long curly eyelashes
Long curly eyelashes
1 1 1 0.12 1 3.8E-03
Chromosome 5p13 Duplication Syndrome
1 0 1 0.12 0 0
CUI: C3550903
Disease: CORNELIA DE LANGE SYNDROME 5
CORNELIA DE LANGE SYNDROME 5
1 0 1 0.12 0 0
CUI: C3552501
Disease: Talus valgus
Talus valgus
1 0 1 0.12 0 0
CUI: C4015466
Disease: Bilateral clinodactyly
Bilateral clinodactyly
1 1 1 0.12 1 3.8E-03
CUI: C4025295
Disease: Elbow hypertrichosis
Elbow hypertrichosis
1 0 1 0.12 0 0
CUI: C4280757
Disease: Fast-growing nails
Fast-growing nails
1 0 1 0.12 0 0
CUI: C4310702
Disease: ALAZAMI-YUAN SYNDROME
ALAZAMI-YUAN SYNDROME
1 2 1 0.12 1 3.7E-03
CUI: C4531263
Disease: Abnormal incisura morphology
Abnormal incisura morphology
1 0 1 0.12 0 0
CUI: C4546640
Disease: Hypertrichosis cubiti short stature
Hypertrichosis cubiti short stature
1 0 1 0.12 0 0
CUI: C0158621
Disease: Congenital subaortic stenosis
Congenital subaortic stenosis
2 0 1 0.11 0 0
Reduced renal corticomedullary differentiation
2 0 1 0.11 0 0
CUI: C4021695
Disease: Hypoplastic radial head
Hypoplastic radial head
2 0 1 0.11 0 0
CUI: C4025234
Disease: Duplication of internal organs
Duplication of internal organs
2 0 1 0.11 0 0
CUI: C4521563
Disease: SPINOCEREBELLAR ATAXIA 44
SPINOCEREBELLAR ATAXIA 44
2 0 1 0.11 0 0
Amphetamine or related acting sympathomimetic abuse
3 0 1 1.0E-01 0 0
CUI: C0155536
Disease: Paracousis
Paracousis
3 0 1 1.0E-01 0 0
CUI: C0260662
Disease: Hearing problem
Hearing problem
3 0 1 1.0E-01 0 0