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: C0375536
Disease: Congenital osteodystrophy
Congenital osteodystrophy
1 0 1 0.33 0 0
CUI: C0432231
Disease: Nievergelt syndrome
Nievergelt syndrome
1 0 1 0.33 0 0
CUI: C1851988
Disease: Dorsal subluxation of ulna
Dorsal subluxation of ulna
1 0 1 0.33 0 0
CUI: C1855276
Disease: Dorsolateral bowed, short radii
Dorsolateral bowed, short radii
1 0 1 0.33 0 0
CUI: C4025460
Disease: Broad ulna
Broad ulna
1 0 1 0.33 0 0
CUI: C4025745
Disease: Abnormal metatarsal morphology
Abnormal metatarsal morphology
1 0 1 0.33 0 0
CUI: C4531241
Disease: Triangular tibia
Triangular tibia
1 0 1 0.33 0 0
CUI: C4551978
Disease: Short forearm
Short forearm
1 0 1 0.33 0 0
CUI: C4706613
Disease: SHOX-related short stature
SHOX-related short stature
1 0 1 0.33 0 0
CUI: C0796021
Disease: Lowry Wood syndrome
Lowry Wood syndrome
2 0 1 0.25 0 0
MESOMELIC DYSPLASIA, KANTAPUTRA TYPE
2 0 1 0.25 0 0
CUI: C1844706
Disease: Rudimentary fibula
Rudimentary fibula
2 0 1 0.25 0 0
CUI: C1855274
Disease: Mesomelic short stature
Mesomelic short stature
2 0 1 0.25 0 0
CUI: C1855277
Disease: Shortening of the tibia
Shortening of the tibia
2 0 1 0.25 0 0
CUI: C1855299
Disease: Forearm undergrowth
Forearm undergrowth
2 0 1 0.25 0 0
CUI: C1855478
Disease: Increased carrying angle
Increased carrying angle
2 0 1 0.25 0 0
CUI: C2910315
Disease: Split foot, bilateral
Split foot, bilateral
2 0 1 0.25 0 0
CUI: C1840088
Disease: Limited wrist movement
Limited wrist movement
3 0 1 0.20 0 0
Mesomelic/rhizomelic limb shortening
3 0 1 0.20 0 0
CUI: C1859860
Disease: Episodic ketoacidosis
Episodic ketoacidosis
4 0 1 0.17 0 0
CUI: C1856732
Disease: Aplasia/Hypoplasia of the fibula
Aplasia/Hypoplasia of the fibula
5 0 1 0.14 0 0
CUI: C0345371
Disease: Hypoplasia of lower limb
Hypoplasia of lower limb
6 0 1 0.12 0 0
CUI: C1840535
Disease: Abnormality of the carpal bones
Abnormality of the carpal bones
6 0 1 0.12 0 0
CUI: C1960539
Disease: Aromatase deficiency
Aromatase deficiency
6 0 1 0.12 0 0
CUI: C0036868
Disease: Sex Chromosome Aberrations
Sex Chromosome Aberrations
8 0 1 1.0E-01 0 0