Source: CLINVAR ×
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: C1844813
Disease: Widely spaced teeth
Widely spaced teeth 		10 10 1 3.6E-02 1 3.1E-02
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		19 0 1 2.7E-02 0 0
CUI: C1866134
Disease: Wide anterior fontanel
Wide anterior fontanel 		6 0 1 4.2E-02 0 0
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		22 27 2 5.1E-02 3 6.4E-02
CUI: C0234860
Disease: Weak cry
Weak cry 		5 4 1 4.3E-02 1 3.8E-02
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		15 0 1 3.0E-02 0 0
CUI: C0340279
Disease: Ventricular hypertrophy
Ventricular hypertrophy 		3 0 1 4.8E-02 0 0
CUI: C0007873
Disease: Uterine Cervical Neoplasm
Uterine Cervical Neoplasm 		16 0 1 2.9E-02 0 0
CUI: C0280630
Disease: Uterine Carcinosarcoma
Uterine Carcinosarcoma 		12 0 2 6.9E-02 0 0
CUI: C0042024
Disease: Urinary Incontinence
Urinary Incontinence 		12 14 1 3.3E-02 1 2.8E-02
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		21 0 1 2.6E-02 0 0
CUI: C0431664
Disease: Unilateral Cryptorchidism
Unilateral Cryptorchidism 		3 0 1 4.8E-02 0 0
CUI: C0231678
Disease: Ulnar deviation of the wrist
Ulnar deviation of the wrist 		5 9 1 4.3E-02 1 3.2E-02
CUI: C0241521
Disease: Ulnar deviation of hand
Ulnar deviation of hand 		0 2 0 0 1 4.2E-02
CUI: C1856202
Disease: U-Shaped upper lip vermilion
U-Shaped upper lip vermilion 		2 0 1 5.0E-02 0 0
CUI: C1835884
Disease: Triangular face
Triangular face 		13 16 1 3.2E-02 1 2.6E-02
CUI: C0279680
Disease: Transitional cell carcinoma of bladder
Transitional cell carcinoma of bladder 		26 0 1 2.3E-02 0 0
CUI: C0040485
Disease: Torticollis
Torticollis 		9 8 1 3.7E-02 1 3.3E-02
CUI: C0040433
Disease: Tooth Crowding
Tooth Crowding 		9 0 1 3.7E-02 0 0
CUI: C0575897
Disease: Thumb deformity
Thumb deformity 		6 7 1 4.2E-02 1 3.4E-02
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		35 0 1 1.9E-02 0 0
CUI: C3150939
Disease: THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome
THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome 		1 10 1 5.3E-02 2 6.5E-02
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		18 0 2 5.7E-02 0 0
CUI: C0578038
Disease: Thin lips
Thin lips 		8 8 1 3.8E-02 1 3.3E-02
CUI: C4024168
Disease: Thickened ears
Thickened ears 		1 0 1 5.3E-02 0 0