NECTIN4, nectin cell adhesion molecule 4, 81607

N. diseases: 77; N. variants: 6
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: C0039075
Disease: Syndactyly
Syndactyly 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 127 26 0.020 None 1.000 2 2014 2018
CUI: C0158646
Disease: Cleft palate with cleft lip
Cleft palate with cleft lip 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 119 43 0.010 None 1.000 1 2014 2014
CUI: C0266037
Disease: Peg-shaped teeth
Peg-shaped teeth 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 17 2 0.100 None 0
CUI: C0432040
Disease: Simple syndactyly of toes, first web space
Simple syndactyly of toes, first web space 		disease Congenital Abnormality 5 3 0.100 None 0
CUI: C1848192
Disease: Absent facial hair
Absent facial hair 		phenotype Congenital Abnormality 3 0.100 None 0
CUI: C4021254
Disease: Cutaneous finger syndactyly
Cutaneous finger syndactyly 		disease Congenital Abnormality 20 1 0.100 None 0
CUI: C0025007
Disease: Measles
Measles 		disease Infections Disease or Syndrome 113 6 0.070 None 1.000 7 2011 2018
CUI: C0012754
Disease: Distemper
Distemper 		disease Infections; Animal Diseases Disease or Syndrome 12 0.040 None 1.000 4 2014 2017
CUI: C3150807
Disease: ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1
ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 		disease Disease or Syndrome 1 6 0.730 strong 1.000 4 6 2010 2018
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 71 16 0.130 None 1.000 3 2011 2018
CUI: C4749852
Disease: Ectodermal dysplasia syndactyly syndrome
Ectodermal dysplasia syndactyly syndrome 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 1 0.030 None 1.000 3 2010 2015
CUI: C0013537
Disease: Eclampsia
Eclampsia 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 241 38 0.010 None 1.000 1 2018 2018
CUI: C0014175
Disease: Endometriosis
Endometriosis 		disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 1188 274 0.010 None 1.000 1 2012 2012
CUI: C0032371
Disease: Poliomyelitis
Poliomyelitis 		disease Infections; Nervous System Diseases Disease or Syndrome 23 0.010 None 1.000 1 2013 2013
CUI: C0038522
Disease: Subacute Sclerosing Panencephalitis
Subacute Sclerosing Panencephalitis 		disease Infections; Nervous System Diseases Disease or Syndrome 47 6 0.010 None 1.000 1 2018 2018
CUI: C0042769
Disease: Virus Diseases
Virus Diseases 		group Infections Disease or Syndrome 1471 42 0.010 None 1.000 1 2013 2013
CUI: C0011351
Disease: Dental Enamel Hypoplasia
Dental Enamel Hypoplasia 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Disease or Syndrome 72 1 0.100 None 0
CUI: C4023710
Disease: Palmar hyperkeratosis
Palmar hyperkeratosis 		disease Disease or Syndrome 6 0.100 None 0
CUI: C0263491
Disease: Pili Torti
Pili Torti 		phenotype Skin and Connective Tissue Diseases Finding 12 0.100 None 0
CUI: C0277959
Disease: Coarse hair
Coarse hair 		phenotype Finding 60 4 0.100 None 0
CUI: C1837279
Disease: Hypoplastic toenails
Hypoplastic toenails 		phenotype Finding 42 1 0.100 None 0
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes 		phenotype Finding 60 4 0.100 None 0
CUI: C1844813
Disease: Widely spaced teeth
Widely spaced teeth 		phenotype Finding 71 10 0.100 None 0
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		phenotype Finding 85 7 0.100 None 0
CUI: C1862862
Disease: Patchy alopecia
Patchy alopecia 		phenotype Skin and Connective Tissue Diseases Finding 8 0.100 None 0