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: C0523827
Disease: Inorganic phosphate measurement
Inorganic phosphate measurement
11 17 11 1.00 17 1.00
Oncogenic hypophosphataemic osteomalacia
5 0 2 0.14 0 0
CUI: C4551565
Disease: Rachitic rosary
Rachitic rosary
7 0 2 0.12 0 0
CUI: C1845169
Disease: Renal phosphate wasting
Renal phosphate wasting
8 0 2 0.12 0 0
Autosomal dominant hypophosphatemic rickets
11 0 2 1.0E-01 0 0
Childhood hypophosphatasia (disorder)
1 0 1 9.1E-02 0 0
CUI: C0234022
Disease: Anorgasmia
Anorgasmia
1 0 1 9.1E-02 0 0
CUI: C1840322
Disease: ODONTOHYPOPHOSPHATASIA (disorder)
ODONTOHYPOPHOSPHATASIA (disorder)
1 0 1 9.1E-02 0 0
Exfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like
1 0 1 9.1E-02 0 0
CUI: C1843983
Disease: Trapezoidal distal femoral condyles
Trapezoidal distal femoral condyles
1 0 1 9.1E-02 0 0
CUI: C1843985
Disease: Shortening of the talar neck
Shortening of the talar neck
1 0 1 9.1E-02 0 0
CUI: C1843986
Disease: Flattening of the talar dome
Flattening of the talar dome
1 0 1 9.1E-02 0 0
Skin dimple over apex of long bone angulation
1 0 1 9.1E-02 0 0
CUI: C2673477
Disease: Hypophosphatasia, Perinatal Lethal
Hypophosphatasia, Perinatal Lethal
1 0 1 9.1E-02 0 0
Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
1 0 1 9.1E-02 0 0
CUI: C3150652
Disease: FANCONI RENOTUBULAR SYNDROME 2
FANCONI RENOTUBULAR SYNDROME 2
1 0 1 9.1E-02 0 0
CUI: C4023157
Disease: Elevated plasma pyrophosphate
Elevated plasma pyrophosphate
1 0 1 9.1E-02 0 0
CUI: C4025607
Disease: Elevated urine pyrophosphate
Elevated urine pyrophosphate
1 0 1 9.1E-02 0 0
CUI: C4225407
Disease: PEELING SKIN SYNDROME 4
PEELING SKIN SYNDROME 4
1 0 1 9.1E-02 0 0
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66
1 0 1 9.1E-02 0 0
CUI: C0268709
Disease: Renal tubular defect
Renal tubular defect
2 0 1 8.3E-02 0 0
Hypophosphatemic Rickets, X-Linked Recessive
2 0 1 8.3E-02 0 0
CUI: C1855828
Disease: Vertebral clefting
Vertebral clefting
2 0 1 8.3E-02 0 0
CUI: C1860202
Disease: Unossified vertebral bodies
Unossified vertebral bodies
2 0 1 8.3E-02 0 0
CUI: C3554055
Disease: PEROXISOME BIOGENESIS DISORDER 14B
PEROXISOME BIOGENESIS DISORDER 14B
2 0 1 8.3E-02 0 0