Source: ALL
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: C4755264
Disease: Severe intellectual disability and progressive spastic paraplegia
Severe intellectual disability and progressive spastic paraplegia 		5 0 4 0.31 0 0
CUI: C3151056
Disease: SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE 		3 0 3 0.25 0 0
CUI: C3279743
Disease: SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 52, AUTOSOMAL RECESSIVE 		3 0 3 0.25 0 0
CUI: C0037020
Disease: Shyness
Shyness 		9 0 4 0.24 0 0
CUI: C0406702
Disease: Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive 		4 0 3 0.23 0 0
CUI: C1844605
Disease: Periorbital wrinkles
Periorbital wrinkles 		5 0 3 0.21 0 0
CUI: C1844606
Disease: Periorbital hyperpigmentation
Periorbital hyperpigmentation 		5 0 3 0.21 0 0
CUI: C1720965
Disease: Ectodermal Dysplasia 3, Anhidrotic
Ectodermal Dysplasia 3, Anhidrotic 		2 0 2 0.17 0 0
CUI: C0393995
Disease: Quadriplegic cerebral palsy
Quadriplegic cerebral palsy 		3 0 2 0.15 0 0
CUI: C3279738
Disease: SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE 		3 0 2 0.15 0 0
CUI: C0265331
Disease: Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) 		4 0 2 0.14 0 0
CUI: C0158486
Disease: Acquired genu recurvatum
Acquired genu recurvatum 		23 0 4 0.13 0 0
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 5 0.12 0 0
CUI: C0152235
Disease: Congenital genu recurvatum
Congenital genu recurvatum 		26 0 4 0.12 0 0
CUI: C0497406
Disease: Overweight
Overweight 		27 0 4 0.11 0 0
CUI: C1839264
Disease: SPASTIC PARAPLEGIA 2, X-LINKED (disorder)
SPASTIC PARAPLEGIA 2, X-LINKED (disorder) 		8 0 2 0.11 0 0
CUI: C3541517
Disease: ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT 		18 0 3 0.11 0 0
CUI: C3888065
Disease: ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT 		18 0 3 0.11 0 0
CUI: C0231274
Disease: Intolerant of heat
Intolerant of heat 		19 0 3 0.11 0 0
CUI: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic 		30 0 4 0.11 0 0
CUI: C0546964
Disease: Genu recurvatum
Genu recurvatum 		32 0 4 1.0E-01 0 0
CUI: C3539920
Disease: ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 11B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 3 8.8E-02 0 0
CUI: C3887494
Disease: ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE 		25 0 3 8.8E-02 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 8.3E-02 0 0
CUI: C0235357
Disease: Hypoplasia of teeth
Hypoplasia of teeth 		14 0 2 8.3E-02 0 0