Source: ALL
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: 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
CUI: C2750066
Disease: Spondylo-Megaepiphyseal-Metaphyseal Dysplasia
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
CUI: C4012268
Disease: TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE
TETRAAMELIA SYNDROME, AUTOSOMAL RECESSIVE 		1 0 1 0.12 0 0
CUI: C4021245
Disease: Patchy variation in bone mineral density
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
CUI: C4319565
Disease: Microcephalic osteodysplastic primordial dwarfism types I and III
Microcephalic osteodysplastic primordial dwarfism types I and III 		1 0 1 0.12 0 0
CUI: C4551965
Disease: ANAUXETIC DYSPLASIA 1
ANAUXETIC DYSPLASIA 1 		1 0 1 0.12 0 0
CUI: C4747922
Disease: PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES
PELGER-HUET ANOMALY WITH MILD SKELETAL ANOMALIES 		1 0 1 0.12 0 0
CUI: C4747923
Disease: TETRAAMELIA SYNDROME 2
TETRAAMELIA SYNDROME 2 		1 0 1 0.12 0 0
CUI: C4747940
Disease: HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY
HUMEROFEMORAL HYPOPLASIA WITH RADIOTIBIAL RAY DEFICIENCY 		1 0 1 0.12 0 0
CUI: C1863353
Disease: Hypoplastic vertebral bodies
Hypoplastic vertebral bodies 		11 0 2 0.12 0 0
CUI: C4021777
Disease: Abnormality of the larynx
Abnormality of the larynx 		11 0 2 0.12 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 0.11 0 0
CUI: C0266273
Disease: Congenital absence of adrenal gland
Congenital absence of adrenal gland 		2 0 1 0.11 0 0
CUI: C0432194
Disease: Schneckenbecken dysplasia
Schneckenbecken dysplasia 		2 0 1 0.11 0 0
CUI: C0796021
Disease: Lowry Wood syndrome
Lowry Wood syndrome 		2 0 1 0.11 0 0
CUI: C1696466
Disease: Hepatic calcification
Hepatic calcification 		2 0 1 0.11 0 0
CUI: C1846059
Disease: Roifman syndrome
Roifman syndrome 		2 0 1 0.11 0 0