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: 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
CUI: C3281203
Disease: CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL
CUTANEOUS TELANGIECTASIA AND CANCER SYNDROME, FAMILIAL 		1 0 1 1.9E-02 0 0
CUI: C3281247
Disease: BENT BONE DYSPLASIA SYNDROME
BENT BONE DYSPLASIA SYNDROME 		1 0 1 1.9E-02 0 0
CUI: C4014656
Disease: CARDIOMYOPATHY, DILATED, 1NN
CARDIOMYOPATHY, DILATED, 1NN 		1 0 1 1.9E-02 0 0
CUI: C4014833
Disease: IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES 		1 0 1 1.9E-02 0 0
CUI: C4693367
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 58 		1 0 1 1.9E-02 0 0
CUI: C4693523
Disease: AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24
AMYOTROPHIC LATERAL SCLEROSIS, SUSCEPTIBILITY TO, 24 		1 0 1 1.9E-02 0 0
CUI: C0022603
Disease: Seborrheic keratosis
Seborrheic keratosis 		2 0 1 1.8E-02 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		2 0 1 1.8E-02 0 0
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		2 0 1 1.8E-02 0 0
CUI: C0795998
Disease: JACKSON-WEISS SYNDROME
JACKSON-WEISS SYNDROME 		2 0 1 1.8E-02 0 0
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		2 0 1 1.8E-02 0 0