Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Severe intellectual disability and progressive spastic paraplegia
5 0 4 0.40 0 0
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE
3 0 3 0.33 0 0
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE
3 0 3 0.33 0 0
CUI: C4023698
Disease: Everted upper lip vermilion
Everted upper lip vermilion
12 0 4 0.24 0 0
CUI: C0393995
Disease: Quadriplegic cerebral palsy
Quadriplegic cerebral palsy
3 0 2 0.20 0 0
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE
3 0 2 0.20 0 0
CUI: C0158486
Disease: Acquired genu recurvatum
Acquired genu recurvatum
23 0 4 0.14 0 0
SPASTIC PARAPLEGIA 2, X-LINKED (disorder)
8 0 2 0.13 0 0
CUI: C0152235
Disease: Congenital genu recurvatum
Congenital genu recurvatum
26 0 4 0.13 0 0
CUI: C0497406
Disease: Overweight
Overweight
27 0 4 0.12 0 0
CUI: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic
30 0 4 0.11 0 0
CUI: C0007939
Disease: Syphilitic chancre
Syphilitic chancre
1 0 1 0.11 0 0
CUI: C0302874
Disease: Depressive personality disorder
Depressive personality disorder
1 0 1 0.11 0 0
CUI: C0751575
Disease: Paralysis, Unilateral, Vocal Cord
Paralysis, Unilateral, Vocal Cord
1 0 1 0.11 0 0
CUI: C2931317
Disease: Primary syphilis
Primary syphilis
1 0 1 0.11 0 0
Synostosis involving the 1st metacarpal
1 0 1 0.11 0 0
Generalized reticulate brown pigmentation
1 0 1 0.11 0 0
MENTAL RETARDATION, X-LINKED, SYNDROMIC 34
1 0 1 0.11 0 0
CUI: C4283894
Disease: MENTAL RETARDATION, X-LINKED 61
MENTAL RETARDATION, X-LINKED 61
1 0 1 0.11 0 0
CUI: C4304578
Disease: 1p21.3 microdeletion syndrome
1p21.3 microdeletion syndrome
1 0 1 0.11 0 0
X-linked intellectual disability Van Esch type
1 0 1 0.11 0 0
CUI: C4478462
Disease: Severe feeding problems
Severe feeding problems
1 0 1 0.11 0 0
CUI: C4732800
Disease: Infantile constant exotropia
Infantile constant exotropia
1 0 1 0.11 0 0
CUI: C0546964
Disease: Genu recurvatum
Genu recurvatum
32 0 4 0.11 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia
33 0 4 0.11 0 0