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: C4553157
Disease: Interleukin 1 Receptor-Like 1 Measurement
Interleukin 1 Receptor-Like 1 Measurement 		5 0 2 0.13 0 0
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		1 0 1 8.3E-02 0 0
CUI: C0495694
Disease: Dysarthria and anarthria
Dysarthria and anarthria 		1 0 1 8.3E-02 0 0
CUI: C1849926
Disease: Phenylpyruvic acidemia
Phenylpyruvic acidemia 		1 0 1 8.3E-02 0 0
CUI: C2678416
Disease: Hyperphenylalaninemia, Non-Pku Mild
Hyperphenylalaninemia, Non-Pku Mild 		1 0 1 8.3E-02 0 0
CUI: C3554428
Disease: OSTEOGENESIS IMPERFECTA, TYPE XIV
OSTEOGENESIS IMPERFECTA, TYPE XIV 		1 0 1 8.3E-02 0 0
CUI: C4016882
Disease: SPASTIC PARAPLEGIA 4, MODIFIER OF
SPASTIC PARAPLEGIA 4, MODIFIER OF 		1 0 1 8.3E-02 0 0
CUI: C4022014
Disease: Maternal hyperphenylalaninemia
Maternal hyperphenylalaninemia 		1 0 1 8.3E-02 0 0
CUI: C4023059
Disease: Chondroitin sulfate excretion in urine
Chondroitin sulfate excretion in urine 		1 0 1 8.3E-02 0 0
CUI: C4025094
Disease: Reduced phenylalanine hydroxylase activity
Reduced phenylalanine hydroxylase activity 		1 0 1 8.3E-02 0 0
CUI: C4025273
Disease: Atypical hyperphenylalaninemia
Atypical hyperphenylalaninemia 		1 0 1 8.3E-02 0 0
CUI: C4280737
Disease: Large elbow
Large elbow 		1 0 1 8.3E-02 0 0
CUI: C4748869
Disease: MIRROR MOVEMENTS 4
MIRROR MOVEMENTS 4 		1 0 1 8.3E-02 0 0
CUI: C0858992
Disease: Pain after application
Pain after application 		2 0 1 7.7E-02 0 0
CUI: C1838192
Disease: SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder)
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT (disorder) 		2 0 1 7.7E-02 0 0
CUI: C1853247
Disease: SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT
SPASTIC PARAPLEGIA 31, AUTOSOMAL DOMINANT 		2 0 1 7.7E-02 0 0
CUI: C1854783
Disease: Grayish enamel
Grayish enamel 		2 0 1 7.7E-02 0 0
CUI: C1854785
Disease: Constricted iliac wings
Constricted iliac wings 		2 0 1 7.7E-02 0 0
CUI: C1854786
Disease: Epiphyseal deformities of tubular bones
Epiphyseal deformities of tubular bones 		2 0 1 7.7E-02 0 0
CUI: C1854787
Disease: Pointed proximal second through fifth metacarpals
Pointed proximal second through fifth metacarpals 		2 0 1 7.7E-02 0 0
CUI: C1863704
Disease: Spastic paraplegia 8, autosomal dominant
Spastic paraplegia 8, autosomal dominant 		2 0 1 7.7E-02 0 0
CUI: C2931441
Disease: Hereditary spastic paralysis, infantile onset ascending
Hereditary spastic paralysis, infantile onset ascending 		2 0 1 7.7E-02 0 0
CUI: C3697982
Disease: Pulmonary arterial hypertension associated with connective tissue disease
Pulmonary arterial hypertension associated with connective tissue disease 		2 0 1 7.7E-02 0 0
CUI: C0458385
Disease: Site-specific infective disorders of skin
Site-specific infective disorders of skin 		3 0 1 7.1E-02 0 0
CUI: C1283601
Disease: Deficiency of sulfatase
Deficiency of sulfatase 		3 0 1 7.1E-02 0 0