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: C4225268
Disease: CUTIS LAXA, AUTOSOMAL DOMINANT 3
CUTIS LAXA, AUTOSOMAL DOMINANT 3
1 3 1 1.00 1 0.17
SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE
1 0 1 1.00 0 0
CUI: C0268354
Disease: De Barsy syndrome
De Barsy syndrome
2 12 1 0.50 1 6.7E-02
CUI: C0392477
Disease: Congenital flat foot
Congenital flat foot
2 0 1 0.50 0 0
CUI: C1112321
Disease: Congenital cutis laxa
Congenital cutis laxa
2 0 1 0.50 0 0
SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE (disorder)
2 0 1 0.50 0 0
Cutis Laxa, Autosomal Recessive, Type IIB
2 0 1 0.50 0 0
Abnormality of the dorsal column of the spinal cord
2 0 1 0.50 0 0
CUI: C4476943
Disease: Impaired continence
Impaired continence
2 0 1 0.50 0 0
CUI: C0268350
Disease: Cutis Laxa, Autosomal Dominant
Cutis Laxa, Autosomal Dominant
3 0 1 0.33 0 0
Atrophy of quadriceps femoris muscle
3 1 1 0.33 1 0.25
CUI: C0264133
Disease: Acquired flat foot
Acquired flat foot
4 0 1 0.25 0 0
Dysfunction of lateral corticospinal tracts
4 0 1 0.25 0 0
CUI: C1848771
Disease: Prominent superficial blood vessels
Prominent superficial blood vessels
4 0 1 0.25 0 0
CUI: C1395674
Disease: Bowel diverticulosis
Bowel diverticulosis
5 0 1 0.20 0 0
CUI: C0042023
Disease: Increased frequency of micturition
Increased frequency of micturition
6 0 1 0.17 0 0
CUI: C4023691
Disease: Abnormality of pain sensation
Abnormality of pain sensation
6 0 1 0.17 0 0
CUI: C0268540
Disease: HHH syndrome
HHH syndrome
8 0 1 0.12 0 0
CUI: C1846017
Disease: Progressive pes cavus
Progressive pes cavus
9 0 1 0.11 0 0
Impaired vibration sensation at ankles
9 0 1 0.11 0 0
CUI: C0410935
Disease: Wide cranial sutures
Wide cranial sutures
10 0 1 1.0E-01 0 0
CUI: C1836843
Disease: Progressive inability to walk
Progressive inability to walk
10 0 1 1.0E-01 0 0
CUI: C1863749
Disease: Carpal bone hypoplasia
Carpal bone hypoplasia
10 0 1 1.0E-01 0 0
CUI: C0234517
Disease: Anarthria speech disorder
Anarthria speech disorder
11 0 1 9.1E-02 0 0
CUI: C1837761
Disease: Narrow nasal ridge
Narrow nasal ridge
11 0 1 9.1E-02 0 0