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: C0342136
Disease: Autonomous thyroid function
Autonomous thyroid function
1 0 1 2.9E-02 0 0
Congenital hypothyroidism with ectopic thyroid
1 0 1 2.9E-02 0 0
CUI: C0342194
Disease: Thyroid Dyshormonogenesis 3
Thyroid Dyshormonogenesis 3
1 0 1 2.9E-02 0 0
CUI: C0343495
Disease: Lockjaw
Lockjaw
1 0 1 2.9E-02 0 0
CUI: C0349619
Disease: Medulloblastoma of cerebellum
Medulloblastoma of cerebellum
1 0 1 2.9E-02 0 0
CUI: C0395941
Disease: Mondini defect
Mondini defect
1 0 1 2.9E-02 0 0
Hearing loss associated with syndrome
1 0 1 2.9E-02 0 0
CUI: C0473223
Disease: Aluminum intoxication
Aluminum intoxication
1 0 1 2.9E-02 0 0
CUI: C0473577
Disease: Eccrine nevus
Eccrine nevus
1 0 1 2.9E-02 0 0
Porokeratotic eccrine ostial and dermal duct nevus
1 0 1 2.9E-02 0 0
CUI: C0473582
Disease: Hair follicle nevus
Hair follicle nevus
1 0 1 2.9E-02 0 0
CUI: C0478084
Disease: Other congenital ichthyosis
Other congenital ichthyosis
1 0 1 2.9E-02 0 0
CUI: C0520758
Disease: Prolonged neuromuscular block
Prolonged neuromuscular block
1 0 1 2.9E-02 0 0
CUI: C0541957
Disease: Fasciculation, Skeletal Muscle
Fasciculation, Skeletal Muscle
1 0 1 2.9E-02 0 0
Follicular occlusion triad - hidradenitis, acne conglobata, dissecting cellulitis of scalp
1 0 1 2.9E-02 0 0
CUI: C0571550
Disease: Allergy to vaccine
Allergy to vaccine
1 0 1 2.9E-02 0 0
CUI: C0585473
Disease: Chondromyxoid fibroma of bone
Chondromyxoid fibroma of bone
1 0 1 2.9E-02 0 0
CUI: C0747602
Disease: pituitary incidentaloma
pituitary incidentaloma
1 0 1 2.9E-02 0 0
CUI: C0749470
Disease: Thyroid cold nodule
Thyroid cold nodule
1 0 1 2.9E-02 0 0
CUI: C0751144
Disease: Fasciculation, Benign
Fasciculation, Benign
1 0 1 2.9E-02 0 0
Deafness, congenital onychodystrophy, recessive form
1 0 1 2.9E-02 0 0
CUI: C0869147
Disease: Neonatal hyperthyroidism
Neonatal hyperthyroidism
1 0 1 2.9E-02 0 0
Posterior Leukoencephalopathy Syndrome
1 0 1 2.9E-02 0 0
CUI: C1112776
Disease: Thyroid hyperplasia
Thyroid hyperplasia
1 0 1 2.9E-02 0 0
CUI: C1262098
Disease: Congenital hyperthyroidism
Congenital hyperthyroidism
1 0 1 2.9E-02 0 0