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: C1835697
Disease: Keratitis Fugax Hereditaria
Keratitis Fugax Hereditaria 		1 0 1 3.8E-02 0 0
CUI: C1846529
Disease: CONE-ROD DYSTROPHY 10
CONE-ROD DYSTROPHY 10 		1 0 1 3.8E-02 0 0
CUI: C1853214
Disease: RETINITIS PIGMENTOSA 35
RETINITIS PIGMENTOSA 35 		1 0 1 3.8E-02 0 0
CUI: C1855459
Disease: Congenital symmetrical palmoplantar keratosis
Congenital symmetrical palmoplantar keratosis 		1 0 1 3.8E-02 0 0
CUI: C1855644
Disease: Keratoderma, Palmoplantar, Norrbotten Recessive Type
Keratoderma, Palmoplantar, Norrbotten Recessive Type 		1 0 1 3.8E-02 0 0
CUI: C1857144
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE 1 		1 0 1 3.8E-02 0 0
CUI: C1866510
Disease: Discolored lateral incisors
Discolored lateral incisors 		1 0 1 3.8E-02 0 0
CUI: C1868633
Disease: Paragangliomas with Sensorineural Hearing Loss
Paragangliomas with Sensorineural Hearing Loss 		1 0 1 3.8E-02 0 0
CUI: C1960046
Disease: Mild persistent asthma
Mild persistent asthma 		1 0 1 3.8E-02 0 0
CUI: C1970027
Disease: Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility
Hypertelorism, Severe, With Midface Prominence, Myopia, Mental Retardation, And Bone Fragility 		1 0 1 3.8E-02 0 0
CUI: C2047516
Disease: Hyperkeratotic papule
Hyperkeratotic papule 		1 0 1 3.8E-02 0 0
CUI: C2363246
Disease: Other specified congenital malformations of skin
Other specified congenital malformations of skin 		1 0 1 3.8E-02 0 0
CUI: C2910342
Disease: Inherited keratosis palmaris et plantaris
Inherited keratosis palmaris et plantaris 		1 0 1 3.8E-02 0 0
CUI: C2910343
Disease: Keratosis follicularis [Darier-White]
Keratosis follicularis [Darier-White] 		1 0 1 3.8E-02 0 0
CUI: C3151445
Disease: DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 		1 0 1 3.8E-02 0 0
CUI: C3276074
Disease: PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS 		1 0 1 3.8E-02 0 0
CUI: C3496177
Disease: Atypical psychosis
Atypical psychosis 		1 0 1 3.8E-02 0 0
CUI: C3532243
Disease: Fatal infantile mitochondrial cardiomyopathy
Fatal infantile mitochondrial cardiomyopathy 		1 0 1 3.8E-02 0 0
CUI: C4022005
Disease: Carotid paraganglioma
Carotid paraganglioma 		1 0 1 3.8E-02 0 0
CUI: C4024828
Disease: Fine, reticulate skin pigmentation
Fine, reticulate skin pigmentation 		1 0 1 3.8E-02 0 0
CUI: C4024891
Disease: Hyperkeratosis with erythema
Hyperkeratosis with erythema 		1 0 1 3.8E-02 0 0
CUI: C4280715
Disease: Decreased level of plasminogen
Decreased level of plasminogen 		1 0 1 3.8E-02 0 0
CUI: C4304594
Disease: 16q24.3 microdeletion syndrome
16q24.3 microdeletion syndrome 		1 0 1 3.8E-02 0 0
CUI: C4304724
Disease: Late-onset junctional epidermolysis bullosa
Late-onset junctional epidermolysis bullosa 		1 0 1 3.8E-02 0 0
CUI: C4476997
Disease: Abnormal B-type natriuretic peptide level
Abnormal B-type natriuretic peptide level 		1 0 1 3.8E-02 0 0