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: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 1 1.4E-03 0 0
CUI: C0020302
Disease: Hydrophthalmos
Hydrophthalmos
60 0 1 1.4E-03 0 0
CUI: C0277959
Disease: Coarse hair
Coarse hair
60 0 1 1.4E-03 0 0
CUI: C1843921
Disease: Postural instability
Postural instability
60 0 1 1.4E-03 0 0
CUI: C0431659
Disease: Hypoplasia of scrotum
Hypoplasia of scrotum
57 0 1 1.4E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance
57 0 1 1.4E-03 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy
56 0 1 1.4E-03 0 0
CUI: C0040485
Disease: Torticollis
Torticollis
55 0 1 1.4E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 1 1.4E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign
54 0 1 1.4E-03 0 0
CUI: C1839546
Disease: Microretrognathia
Microretrognathia
53 0 1 1.4E-03 0 0
CUI: C1853737
Disease: Prominent occiput
Prominent occiput
53 0 1 1.4E-03 0 0
CUI: C1860816
Disease: Preauricular skin tag
Preauricular skin tag
53 0 1 1.4E-03 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs
51 0 1 1.4E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement
50 0 1 1.4E-03 0 0
CUI: C2699510
Disease: Split-Hand/Foot Malformation
Split-Hand/Foot Malformation
50 0 1 1.4E-03 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination
49 0 1 1.4E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 1 1.4E-03 0 0
CUI: C0233844
Disease: Clumsiness
Clumsiness
48 0 1 1.4E-03 0 0
CUI: C0431663
Disease: Bilateral Cryptorchidism
Bilateral Cryptorchidism
48 0 1 1.4E-03 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 1 1.4E-03 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5
48 0 1 1.4E-03 0 0
CUI: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism
48 0 1 1.4E-03 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High
47 0 1 1.4E-03 0 0
CUI: C0001916
Disease: Albinism
Albinism
46 0 1 1.4E-03 0 0