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: C4551851
Disease: Cornelia de Lange Syndrome 1
Cornelia de Lange Syndrome 1
8 0 4 0.18 0 0
CUI: C2673670
Disease: Curly eyelashes
Curly eyelashes
15 0 5 0.18 0 0
CUI: C1849311
Disease: Short 1st metacarpal
Short 1st metacarpal
18 0 5 0.16 0 0
CUI: C0271007
Disease: Phthisis bulbi
Phthisis bulbi
11 0 4 0.16 0 0
CUI: C1849510
Disease: Prenatal movement abnormality
Prenatal movement abnormality
11 0 4 0.16 0 0
Growth Deficiency and Mental Retardation with Facial Dysmorphism
4 0 3 0.16 0 0
Congenital muscular hypertrophy-cerebral syndrome
5 0 3 0.15 0 0
CUI: C1853099
Disease: Cornelia de Lange Syndrome 3
Cornelia de Lange Syndrome 3
5 0 3 0.15 0 0
CUI: C4023915
Disease: Abnormally low-pitched voice
Abnormally low-pitched voice
14 0 4 0.14 0 0
CUI: C3887496
Disease: Oligodactyly
Oligodactyly
20 0 4 0.12 0 0
CUI: C0432355
Disease: Hypoplasia of nipple
Hypoplasia of nipple
33 0 5 0.11 0 0
CUI: C1269700
Disease: Caliectasis
Caliectasis
3 0 2 0.11 0 0
CUI: C1847363
Disease: Aplasia/Hypoplasia of the ribs
Aplasia/Hypoplasia of the ribs
3 0 2 0.11 0 0
CUI: C0566899
Disease: Small labia majora
Small labia majora
35 0 5 0.10 0 0
CUI: C0270972
Disease: Cornelia De Lange Syndrome
Cornelia De Lange Syndrome
48 0 6 1.0E-01 0 0
CUI: C0728895
Disease: Absent finger
Absent finger
26 0 4 1.0E-01 0 0
CUI: C1857641
Disease: Severe postnatal growth retardation
Severe postnatal growth retardation
30 0 4 9.1E-02 0 0
CUI: C4023676
Disease: Increased nuchal translucency
Increased nuchal translucency
30 0 4 9.1E-02 0 0
CUI: C0155158
Disease: Recurrent pterygium
Recurrent pterygium
7 0 2 8.7E-02 0 0
Acute myeloid leukemia, 11q23 abnormalities
7 0 2 8.7E-02 0 0
CUI: C1865572
Disease: Proximal placement of thumb
Proximal placement of thumb
32 0 4 8.7E-02 0 0
CUI: C0266383
Disease: Uterine Anomalies
Uterine Anomalies
35 0 4 8.2E-02 0 0
Leukemia, Megakaryoblastic, of Down Syndrome
9 0 2 8.0E-02 0 0
CUI: C4551560
Disease: Truncal obesity
Truncal obesity
38 0 4 7.7E-02 0 0
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis
67 0 6 7.6E-02 0 0