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: C3553754
Disease: Absent toe
Absent toe 		8 0 6 9.2E-02 0 0
CUI: C0265268
Disease: Adams Oliver syndrome
Adams Oliver syndrome 		9 0 6 9.1E-02 0 0
CUI: C1866141
Disease: Foot dorsiflexor weakness
Foot dorsiflexor weakness 		70 0 11 9.0E-02 0 0
CUI: C1847584
Disease: Distal sensory impairment
Distal sensory impairment 		86 0 12 8.8E-02 0 0
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes 		129 0 15 8.5E-02 0 0
CUI: C3164374
Disease: Abnormality of pulmonary valve
Abnormality of pulmonary valve 		40 0 8 8.4E-02 0 0
CUI: C1856786
Disease: Hypoplastic fingernail
Hypoplastic fingernail 		30 0 7 8.1E-02 0 0
CUI: C4551482
Disease: Adams-Oliver syndrome 1
Adams-Oliver syndrome 1 		17 0 6 8.1E-02 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly 		127 0 14 8.0E-02 0 0
CUI: C0265908
Disease: Congenital atresia of pulmonary artery
Congenital atresia of pulmonary artery 		19 0 6 7.9E-02 0 0
CUI: C1832776
Disease: Hypertrophic nerve changes
Hypertrophic nerve changes 		6 0 5 7.8E-02 0 0
CUI: C1854442
Disease: SPLIT-HAND/FOOT MALFORMATION 4
SPLIT-HAND/FOOT MALFORMATION 4 		6 4 5 7.8E-02 1 0.17
CUI: C1863204
Disease: ADULT SYNDROME
ADULT SYNDROME 		6 0 5 7.8E-02 0 0
CUI: C1408174
Disease: Hypertrophic neuropathy of infancy
Hypertrophic neuropathy of infancy 		21 0 6 7.7E-02 0 0
CUI: C1408182
Disease: Hereditary motor and sensory neuropathy, types I-IV
Hereditary motor and sensory neuropathy, types I-IV 		21 0 6 7.7E-02 0 0
CUI: C1843077
Disease: Segmental peripheral demyelination/remyelination
Segmental peripheral demyelination/remyelination 		21 0 6 7.7E-02 0 0
CUI: C2875300
Disease: Peroneal muscular atrophy (axonal type) (hypertrophic type)
Peroneal muscular atrophy (axonal type) (hypertrophic type) 		21 0 6 7.7E-02 0 0
CUI: C0008441
Disease: Chondroblastoma
Chondroblastoma 		22 0 6 7.6E-02 0 0
CUI: C1856749
Disease: Aplastic/hypoplastic toenail
Aplastic/hypoplastic toenail 		23 0 6 7.5E-02 0 0
CUI: C1838652
Disease: SPLIT-HAND/FOOT MALFORMATION 3
SPLIT-HAND/FOOT MALFORMATION 3 		9 0 5 7.5E-02 0 0
CUI: C4281601
Disease: Foot oligodactyly
Foot oligodactyly 		9 0 5 7.5E-02 0 0
CUI: C0027888
Disease: Hereditary Motor and Sensory Neuropathies
Hereditary Motor and Sensory Neuropathies 		53 0 8 7.4E-02 0 0
CUI: C0003076
Disease: Aniridia
Aniridia 		83 0 10 7.4E-02 0 0
CUI: C0406704
Disease: Rudiger syndrome 1
Rudiger syndrome 1 		10 0 5 7.4E-02 0 0
CUI: C0205713
Disease: Roussy-Levy Syndrome (disorder)
Roussy-Levy Syndrome (disorder) 		26 0 6 7.2E-02 0 0