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: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 8.3E-02 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 8.3E-02 0 0
CUI: C0432125
Disease: Bicoronal craniosynostosis
Bicoronal craniosynostosis 		1 0 1 8.3E-02 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 8.3E-02 0 0
CUI: C0862039
Disease: Precursor B-lymphoblastic lymphoma stage II
Precursor B-lymphoblastic lymphoma stage II 		1 0 1 8.3E-02 0 0
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		1 0 1 8.3E-02 0 0
CUI: C1336727
Disease: Testicular Sarcoma
Testicular Sarcoma 		1 0 1 8.3E-02 0 0
CUI: C1851152
Disease: SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS
SKELETAL DYSPLASIA WITH ACANTHOSIS NIGRICANS 		1 0 1 8.3E-02 0 0
CUI: C1851996
Disease: Dwarfism tall vertebrae
Dwarfism tall vertebrae 		1 0 1 8.3E-02 0 0
CUI: C1861213
Disease: Wide-cupped costochondral junctions
Wide-cupped costochondral junctions 		1 0 1 8.3E-02 0 0
CUI: C1863423
Disease: Lumbar kyphosis in infancy
Lumbar kyphosis in infancy 		1 0 1 8.3E-02 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome 		1 0 1 8.3E-02 0 0
CUI: C1864854
Disease: Broad femoral metaphyses
Broad femoral metaphyses 		1 0 1 8.3E-02 0 0
CUI: C2674171
Disease: Lethal short-limbed short stature
Lethal short-limbed short stature 		1 0 1 8.3E-02 0 0
CUI: C2677099
Disease: CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)
CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder) 		1 0 1 8.3E-02 0 0
CUI: C2678471
Disease: Lethal Arthrogryposis With Anterior Horn Cell Disease
Lethal Arthrogryposis With Anterior Horn Cell Disease 		1 0 1 8.3E-02 0 0
CUI: C2930792
Disease: Familial acanthosis nigricans
Familial acanthosis nigricans 		1 0 1 8.3E-02 0 0
CUI: C2930793
Disease: Achondroplastic dwarfism
Achondroplastic dwarfism 		1 0 1 8.3E-02 0 0
CUI: C3272759
Disease: Brain Development Abnormality
Brain Development Abnormality 		1 0 1 8.3E-02 0 0
CUI: C3280146
Disease: THREE M SYNDROME 3
THREE M SYNDROME 3 		1 0 1 8.3E-02 0 0
CUI: C3552501
Disease: Talus valgus
Talus valgus 		1 0 1 8.3E-02 0 0
CUI: C3554793
Disease: Loose anagen hair
Loose anagen hair 		1 0 1 8.3E-02 0 0
CUI: C3807591
Disease: Widening of cervical spinal canal
Widening of cervical spinal canal 		1 0 1 8.3E-02 0 0
CUI: C3888131
Disease: INCREASED RESPONSIVENESS TO GROWTH HORMONE
INCREASED RESPONSIVENESS TO GROWTH HORMONE 		1 0 1 8.3E-02 0 0
CUI: C4016705
Disease: LARON SYNDROME WITH ELEVATED SERUM GH-BINDING PROTEIN
LARON SYNDROME WITH ELEVATED SERUM GH-BINDING PROTEIN 		1 0 1 8.3E-02 0 0