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: C0332885
Disease: Congenital stenosis
Congenital stenosis
1 0 1 0.12 0 0
CUI: C0432219
Disease: Opsismodysplasia
Opsismodysplasia
1 0 1 0.12 0 0
CUI: C0748397
Disease: Reynolds syndrome
Reynolds syndrome
1 0 1 0.12 0 0
CUI: C0854486
Disease: Secretory adenoma of pituitary
Secretory adenoma of pituitary
1 0 1 0.12 0 0
CUI: C0877313
Disease: Neonatal neuroblastoma
Neonatal neuroblastoma
1 0 1 0.12 0 0
Cutaneous Lymphomatoid Granulomatosis
1 0 1 0.12 0 0
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
1 0 1 0.12 0 0
CUI: C1848877
Disease: Peripheral pulmonary vessel aplasia
Peripheral pulmonary vessel aplasia
1 0 1 0.12 0 0
CUI: C1850644
Disease: Anterior bowing of long bones
Anterior bowing of long bones
1 0 1 0.12 0 0
CUI: C1855205
Disease: Susceptibility to chickenpox
Susceptibility to chickenpox
1 0 1 0.12 0 0
Anterior rib punctate calcifications
1 0 1 0.12 0 0
CUI: C1859121
Disease: Sternal punctate calcifications
Sternal punctate calcifications
1 0 1 0.12 0 0
CUI: C1859458
Disease: Cleft vertebral arch
Cleft vertebral arch
1 0 1 0.12 0 0
CUI: C1859462
Disease: Absent knee epiphyses
Absent knee epiphyses
1 0 1 0.12 0 0
CUI: C1866048
Disease: Severe hydrops fetalis
Severe hydrops fetalis
1 0 1 0.12 0 0
CUI: C2017869
Disease: sparse facial hair
sparse facial hair
1 0 1 0.12 0 0
Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
1 0 1 0.12 0 0
CUI: C3179244
Disease: Pseudo Pelger-Huet Anomaly
Pseudo Pelger-Huet Anomaly
1 0 1 0.12 0 0
TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE
1 0 1 0.12 0 0
Patchy variation in bone mineral density
1 0 1 0.12 0 0
CUI: C4021969
Disease: Abnormally straight spine
Abnormally straight spine
1 0 1 0.12 0 0
CUI: C4024619
Disease: Broad femoral head
Broad femoral head
1 0 1 0.12 0 0
CUI: C4025034
Disease: Abnormality of femoral epiphysis
Abnormality of femoral epiphysis
1 0 1 0.12 0 0
CUI: C4025368
Disease: Pseudoepiphyses of hand bones
Pseudoepiphyses of hand bones
1 0 1 0.12 0 0
CUI: C4025815
Disease: Short diaphyses
Short diaphyses
1 0 1 0.12 0 0