Source: INFERRED

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0079683
Disease: Herlitz Disease
Herlitz Disease
disease 0.810 None 1.000 11 54 1992 2017
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
Adult junctional epidermolysis bullosa (disorder)
disease 0.800 None 1.000 1 3 1994 2017
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1145670
Disease: Respiratory Failure
Respiratory Failure
disease 0.110 None 1.000 0 0 2018 2018
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive
disease 0.110 None 1.000 0 0 2018 2018
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
phenotype 0.100 None 1.000 1 2 2018 2018
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
disease 0.100 None 1.000 1 1 2011 2011
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
phenotype 0.100 None 1.000 1 1 2017 2017
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1856953
Disease: Palmar hyperhidrosis
Palmar hyperhidrosis
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1853193
Disease: Recurrent skin infections
Recurrent skin infections
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C4551676
Disease: Laryngismus stridulus
Laryngismus stridulus
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0152415
Disease: Ankyloglossia
Ankyloglossia
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0853945
Disease: Oral mucosal blisters
Oral mucosal blisters
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1856954
Disease: Plantar hyperkeratosis
Plantar hyperkeratosis
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1856963
Disease: Fragile nails
Fragile nails
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C1858430
Disease: Death in infancy
Death in infancy
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C4551675
Disease: Keratoderma, Palmoplantar
Keratoderma, Palmoplantar
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C4551650
Disease: Esophageal Stricture
Esophageal Stricture
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C4021730
Disease: Junctional split
Junctional split
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C3887524
Disease: Skin Erosion
Skin Erosion
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
CUI: C3806301
Disease: Scarring alopecia of scalp
Scarring alopecia of scalp
phenotype 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
disease 0.100 None 0 0
Entrez Id: 3918
Gene Symbol: LAMC2
LAMC2
laminin subunit gamma 2 0.389 0.923 2.9E-12
Congenital localized absence of skin
disease 0.100 None 0 0