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: C0151934
Disease: Hypogeusia
Hypogeusia
6 0 5 0.42 0 0
Neuropathy, Hereditary Sensory And Autonomic, Type IIA
5 0 4 0.33 0 0
CUI: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis
6 0 4 0.31 0 0
Hereditary Sensory Autonomic Neuropathy, Type 2
8 0 4 0.27 0 0
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury
8 0 4 0.27 0 0
CUI: C1852289
Disease: Autoamputation of digits
Autoamputation of digits
8 0 4 0.27 0 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration
8 0 4 0.27 0 0
CUI: C0079297
Disease: Epidermolysis Bullosa Progressiva
Epidermolysis Bullosa Progressiva
4 0 3 0.25 0 0
CUI: C0478085
Disease: Other epidermolysis bullosa
Other epidermolysis bullosa
4 0 3 0.25 0 0
CUI: C2673610
Disease: JEB-I
JEB-I
4 0 3 0.25 0 0
CUI: C4025676
Disease: Abnormality of the knee
Abnormality of the knee
10 0 4 0.24 0 0
CUI: C1856953
Disease: Palmar hyperhidrosis
Palmar hyperhidrosis
5 0 3 0.23 0 0
EPIDERMOLYSIS BULLOSA, JUNCTIONAL, LOCALISATA VARIANT (disorder)
5 0 3 0.23 0 0
Epidermolysis bullosa inversa dystrophica
5 0 3 0.23 0 0
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
6 0 3 0.21 0 0
Adult junctional epidermolysis bullosa (disorder)
6 0 3 0.21 0 0
Congenital localized absence of skin
6 0 3 0.21 0 0
CUI: C4021730
Disease: Junctional split
Junctional split
6 0 3 0.21 0 0
CUI: C1969236
Disease: Mitten deformity
Mitten deformity
7 0 3 0.20 0 0
CUI: C4551676
Disease: Laryngismus stridulus
Laryngismus stridulus
7 0 3 0.20 0 0
CUI: C0151572
Disease: Reflex, Corneal, Decreased
Reflex, Corneal, Decreased
14 0 4 0.19 0 0
CUI: C4024942
Disease: Late-onset muscular dystrophy
Late-onset muscular dystrophy
8 0 3 0.19 0 0
Decreased sensory nerve conduction velocity
15 0 4 0.18 0 0
CUI: C4528699
Disease: Devil Facial Tumor Disease
Devil Facial Tumor Disease
2 0 2 0.18 0 0
Neonatal inflammatory skin and bowel disease
2 0 2 0.18 0 0