Source: UNIPROT ×
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: C0001080
Disease: Achondroplasia
Achondroplasia 		1 0 1 1.9E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		1 0 1 1.9E-02 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		1 0 1 1.9E-02 0 0
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		1 0 1 1.9E-02 0 0
CUI: C0024507
Disease: Majewski Syndrome
Majewski Syndrome 		1 0 1 1.9E-02 0 0
CUI: C0334634
Disease: Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse 		1 0 1 1.9E-02 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		1 0 1 1.9E-02 0 0
CUI: C1300257
Disease: Thanatophoric dysplasia, type 2
Thanatophoric dysplasia, type 2 		1 0 1 1.9E-02 0 0
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		1 0 1 1.9E-02 0 0
CUI: C1852406
Disease: Cutis Gyrata Syndrome of Beare And Stevenson
Cutis Gyrata Syndrome of Beare And Stevenson 		1 0 1 1.9E-02 0 0
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		1 0 1 1.9E-02 0 0
CUI: C1861065
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 9 		1 0 1 1.9E-02 0 0
CUI: C1863599
Disease: Hereditary Myopathy with Early Respiratory Failure
Hereditary Myopathy with Early Respiratory Failure 		1 0 1 1.9E-02 0 0
CUI: C1864436
Disease: Muenke Syndrome
Muenke Syndrome 		1 0 1 1.9E-02 0 0
CUI: C1864852
Disease: CATSHL syndrome
CATSHL syndrome 		1 0 1 1.9E-02 0 0
CUI: C1865070
Disease: SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION
SCAPHOCEPHALY, MAXILLARY RETRUSION, AND MENTAL RETARDATION 		1 0 1 1.9E-02 0 0
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		1 0 1 1.9E-02 0 0
CUI: C1868678
Disease: THANATOPHORIC DYSPLASIA, TYPE I (disorder)
THANATOPHORIC DYSPLASIA, TYPE I (disorder) 		1 0 1 1.9E-02 0 0
CUI: C1969056
Disease: LEOPARD SYNDROME 2
LEOPARD SYNDROME 2 		1 0 1 1.9E-02 0 0
CUI: C1969057
Disease: Noonan Syndrome 5
Noonan Syndrome 5 		1 0 1 1.9E-02 0 0
CUI: C2674173
Disease: Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans 		1 0 1 1.9E-02 0 0
CUI: C2677099
Disease: CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder)
CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS (disorder) 		1 0 1 1.9E-02 0 0
CUI: C2931196
Disease: Craniofacial dysostosis type 1
Craniofacial dysostosis type 1 		1 0 1 1.9E-02 0 0
CUI: C2936791
Disease: Antley-Bixler Syndrome, Autosomal Dominant
Antley-Bixler Syndrome, Autosomal Dominant 		1 0 1 1.9E-02 0 0
CUI: C3151303
Disease: Obesity, Hyperphagia, and Developmental Delay
Obesity, Hyperphagia, and Developmental Delay 		1 0 1 1.9E-02 0 0