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: C1859162
Disease: Neonatal cholestatic liver disease
Neonatal cholestatic liver disease 		3 0 3 0.11 0 0
CUI: C0549613
Disease: Biliary tract abnormality
Biliary tract abnormality 		14 0 4 0.11 0 0
CUI: C0752323
Disease: Focal Clonic Seizures
Focal Clonic Seizures 		12 0 3 8.3E-02 0 0
CUI: C0432315
Disease: Epidermolysis bullosa simplex herpetiformis
Epidermolysis bullosa simplex herpetiformis 		2 0 2 7.4E-02 0 0
CUI: C3715082
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE 1 		2 0 2 7.4E-02 0 0
CUI: C3875046
Disease: Partial nephrogenic diabetes insipidus
Partial nephrogenic diabetes insipidus 		2 0 2 7.4E-02 0 0
CUI: C4021125
Disease: Secretory adrenocortical adenoma
Secretory adrenocortical adenoma 		2 0 2 7.4E-02 0 0
CUI: C4302031
Disease: Basal epidermolysis bullosa simplex
Basal epidermolysis bullosa simplex 		2 0 2 7.4E-02 0 0
CUI: C0268443
Disease: Acquired Nephrogenic Diabetes Insipidus
Acquired Nephrogenic Diabetes Insipidus 		3 0 2 7.1E-02 0 0
CUI: C1112601
Disease: Hypertonic dehydration
Hypertonic dehydration 		3 0 2 7.1E-02 0 0
CUI: C1563706
Disease: Nephrogenic Diabetes Insipidus, Type II
Nephrogenic Diabetes Insipidus, Type II 		3 0 2 7.1E-02 0 0
CUI: C1850544
Disease: Hypernatremic dehydration
Hypernatremic dehydration 		3 0 2 7.1E-02 0 0
CUI: C3542500
Disease: ADH-Resistant Diabetes Insipidus
ADH-Resistant Diabetes Insipidus 		3 0 2 7.1E-02 0 0
CUI: C1969156
Disease: EEG with burst suppression
EEG with burst suppression 		19 0 3 7.0E-02 0 0
CUI: C0079295
Disease: Epidermolysis Bullosa Herpetiformis Dowling-Meara
Epidermolysis Bullosa Herpetiformis Dowling-Meara 		4 0 2 6.9E-02 0 0
CUI: C0080333
Disease: Weber-Cockayne Syndrome
Weber-Cockayne Syndrome 		4 0 2 6.9E-02 0 0
CUI: C0268293
Disease: Corticosterone Methyl Oxidase Type I Deficiency
Corticosterone Methyl Oxidase Type I Deficiency 		4 0 2 6.9E-02 0 0
CUI: C1832926
Disease: EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder)
EPIDERMOLYSIS BULLOSA SIMPLEX, AUTOSOMAL RECESSIVE (disorder) 		4 0 2 6.9E-02 0 0
CUI: C1839541
Disease: Episodic ammonia intoxication
Episodic ammonia intoxication 		4 0 2 6.9E-02 0 0
CUI: C3463917
Disease: Corticosterone Methyl Oxidase Type II Deficiency
Corticosterone Methyl Oxidase Type II Deficiency 		4 0 2 6.9E-02 0 0
CUI: C4024876
Disease: Palmoplantar blistering
Palmoplantar blistering 		4 0 2 6.9E-02 0 0
CUI: C4025095
Disease: Hypoargininemia
Hypoargininemia 		4 0 2 6.9E-02 0 0
CUI: C0232720
Disease: Pale feces (finding)
Pale feces (finding) 		5 0 2 6.7E-02 0 0
CUI: C0232831
Disease: Impairment of urinary concentration
Impairment of urinary concentration 		5 0 2 6.7E-02 0 0
CUI: C0432316
Disease: Epidermolysis bullosa simplex with mottled pigmentation
Epidermolysis bullosa simplex with mottled pigmentation 		5 0 2 6.7E-02 0 0