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: C1856637
Disease: Spatulate ribs
Spatulate ribs
1 0 1 1.0E-01 0 0
Multicentric ossification of proximal humeral epiphyses
1 0 1 1.0E-01 0 0
Multicentric ossification of proximal femoral epiphyses
1 0 1 1.0E-01 0 0
CUI: C1863734
Disease: Caudal interpedicular narrowing
Caudal interpedicular narrowing
1 0 1 1.0E-01 0 0
CUI: C1866703
Disease: Severe carpal ossification delay
Severe carpal ossification delay
1 0 1 1.0E-01 0 0
CUI: C1867494
Disease: Fragmented, irregular epiphyses
Fragmented, irregular epiphyses
1 0 1 1.0E-01 0 0
CUI: C1868170
Disease: Hypoplasia of deltoid muscle
Hypoplasia of deltoid muscle
1 0 1 1.0E-01 0 0
CUI: C1868616
Disease: Parastremmatic dwarfism
Parastremmatic dwarfism
1 0 1 1.0E-01 0 0
Charcot-Marie-Tooth disease, Type 2C
1 0 1 1.0E-01 0 0
Mucolipidosis III Alpha Beta, Atypical
1 0 1 1.0E-01 0 0
CUI: C2931894
Disease: Mucolipidosis 2
Mucolipidosis 2
1 0 1 1.0E-01 0 0
Childhood-onset short-trunk short stature
1 0 1 1.0E-01 0 0
SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1
1 0 1 1.0E-01 0 0
SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE
1 0 1 1.0E-01 0 0
CUI: C3277114
Disease: Relatively short spine
Relatively short spine
1 0 1 1.0E-01 0 0
CUI: C3277116
Disease: Long coccyx
Long coccyx
1 0 1 1.0E-01 0 0
CUI: C3277119
Disease: Halberd-shaped pelvis
Halberd-shaped pelvis
1 0 1 1.0E-01 0 0
Hyperplasia of the femoral trochanters
1 0 1 1.0E-01 0 0
CUI: C3277123
Disease: Dumbbell-shaped metaphyses
Dumbbell-shaped metaphyses
1 0 1 1.0E-01 0 0
Absent primary metaphyseal spongiosa
1 0 1 1.0E-01 0 0
Abnormal metaphyseal vascular invasion
1 0 1 1.0E-01 0 0
CUI: C3711162
Disease: Metatropic Dysplasia Type 1
Metatropic Dysplasia Type 1
1 0 1 1.0E-01 0 0
EPIPHYSEAL DYSPLASIA, MULTIPLE, 1, SEVERE
1 0 1 1.0E-01 0 0
Small epiphyses of the phalanges of the hand
1 0 1 1.0E-01 0 0
CUI: C4021554
Disease: Irregular tarsal ossification
Irregular tarsal ossification
1 0 1 1.0E-01 0 0