KRT10, keratin 10, 3858

N. diseases: 93; N. variants: 21
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C4511307
Disease: Keratinopathic ichthyosis
Keratinopathic ichthyosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2016 2016
CUI: C0343731
Disease: Penile warts
Penile warts 		phenotype Neoplasms; Infections; Skin and Connective Tissue Diseases; Male Urogenital Diseases Sign or Symptom 2 0.010 None 1.000 1 1998 1998
CUI: C0432307
Disease: Ichthyosis hystrix of Curth-Macklin
Ichthyosis hystrix of Curth-Macklin 		disease Congenital Abnormality 2 0.010 None 1.000 1 2018 2018
CUI: C1836681
Disease: Erythrokeratoderma, Reticular
Erythrokeratoderma, Reticular 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.300 None 1.000 1 2010 2010
CUI: C3665704
Disease: Congenital reticular ichthyosiform erythroderma
Congenital reticular ichthyosiform erythroderma 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 4 6 0.790 strong 1.000 11 5 1994 2019
CUI: C0846967
Disease: Acanthoma
Acanthoma 		disease Neoplasms Neoplastic Process 5 0.010 None 1.000 1 1997 1997
CUI: C1843463
Disease: Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis
Ichthyosis, Cyclic, with Epidermolytic Hyperkeratosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 6 5 0.730 strong 1.000 3 3 1997 1999
CUI: C0079584
Disease: Ichthyosis Vulgaris
Ichthyosis Vulgaris 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome; Congenital Abnormality 10 18 0.010 None 1.000 1 2017 2017
CUI: C4021849
Disease: Conjunctival hamartoma
Conjunctival hamartoma 		disease Disease or Syndrome 10 0.100 None 0
CUI: C0334245
Disease: Intraepithelial Squamous Cell Carcinoma
Intraepithelial Squamous Cell Carcinoma 		disease Pathological Conditions, Signs and Symptoms; Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 12 0.010 None 1.000 1 2018 2018
CUI: C0334082
Disease: NEVUS, EPIDERMAL (disorder)
NEVUS, EPIDERMAL (disorder) 		disease Neoplasms Disease or Syndrome 14 17 0.020 None 1.000 2 1994 2007
CUI: C0265334
Disease: Pachyonychia Congenita
Pachyonychia Congenita 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 18 7 0.300 None 1.000 2 1994 2015
CUI: C1561989
Disease: Limbal stem cell deficiency
Limbal stem cell deficiency 		disease Eye Diseases Disease or Syndrome 19 0.010 None 1.000 1 2019 2019
CUI: C0079153
Disease: Hyperkeratosis, Epidermolytic
Hyperkeratosis, Epidermolytic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 20 35 0.800 None 0.980 49 14 1992 2020
CUI: C0237849
Disease: Peeling of skin
Peeling of skin 		phenotype Finding 21 0.100 None 0
CUI: C0346210
Disease: Vulval intraepithelial neoplasia
Vulval intraepithelial neoplasia 		disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications Neoplastic Process 29 0.010 None 1.000 1 1993 1993
CUI: C0079298
Disease: Epidermolysis Bullosa Simplex
Epidermolysis Bullosa Simplex 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 30 33 0.010 None 1.000 1 1994 1994
CUI: C0265987
Disease: Nevus comedonicus
Nevus comedonicus 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 31 6 0.010 None 1.000 1 2016 2016
CUI: C0011649
Disease: Dermoid Cyst
Dermoid Cyst 		disease Neoplasms Neoplastic Process 33 0.010 None 1.000 1 2007 2007
CUI: C0221270
Disease: Acanthosis
Acanthosis 		phenotype Pathological Conditions, Signs and Symptoms Finding 37 0.100 None 0
CUI: C0022596
Disease: Palmoplantar Keratosis
Palmoplantar Keratosis 		disease Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 39 6 0.100 None 0
CUI: C0848332
Disease: Spots on skin
Spots on skin 		phenotype Skin and Connective Tissue Diseases Sign or Symptom 43 0.010 None 1.000 1 2015 2015
CUI: C1332271
Disease: Perianal Squamous Intraepithelial Neoplasia
Perianal Squamous Intraepithelial Neoplasia 		disease Neoplastic Process 52 0.010 None 1.000 1 2013 2013
CUI: C0221228
Disease: Comedone
Comedone 		disease Skin and Connective Tissue Diseases Disease or Syndrome 53 0.010 None 1.000 1 2016 2016
CUI: C0037277
Disease: Skin Diseases, Genetic
Skin Diseases, Genetic 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 57 6 0.040 None 1.000 4 1999 2019