NECTIN1, nectin cell adhesion molecule 1, 5818

N. diseases: 196; N. variants: 5
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: C1833538
Disease: OROFACIAL CLEFT 7
OROFACIAL CLEFT 7 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 1 1 0.100 None 0 1
CUI: C1857048
Disease: Progressive hypotrichosis
Progressive hypotrichosis 		phenotype Finding 1 0.100 None 0
CUI: C0037140
Disease: B Virus Infection
B Virus Infection 		disease Infections Disease or Syndrome 3 0.300 None 1.000 1 2000 2000
CUI: C3826237
Disease: Head--Tumors
Head--Tumors 		disease Neoplastic Process 3 0.010 None 1.000 1 2018 2018
CUI: C1298692
Disease: Cleft lip and alveolus
Cleft lip and alveolus 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Congenital Abnormality 4 0.300 None 1.000 1 2006 2006
CUI: C0262475
Disease: Congenital abnormality of Eustachian tube
Congenital abnormality of Eustachian tube 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 4 0.100 None 0
CUI: C2931488
Disease: Zlotogora-Ogur syndrome
Zlotogora-Ogur syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Stomatognathic Diseases; Behavior and Behavior Mechanisms Disease or Syndrome 5 4 0.730 None 1.000 5 4 2000 2015
CUI: C1834737
Disease: Cutaneous syndactyly of toes
Cutaneous syndactyly of toes 		disease Congenital Abnormality 5 1 0.100 None 0
CUI: C4023357
Disease: Maternal teratogenic exposure
Maternal teratogenic exposure 		phenotype Finding 5 1 0.100 None 0
CUI: C4025062
Disease: Supernumerary maxillary incisor
Supernumerary maxillary incisor 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Anatomical Abnormality 5 0.100 None 0
CUI: C4025215
Disease: Disturbance of facial expression
Disturbance of facial expression 		phenotype Finding 5 0.100 None 0
CUI: C4316811
Disease: Abnormality of the nasal septum
Abnormality of the nasal septum 		phenotype Anatomical Abnormality 5 1 0.100 None 0
CUI: C1857045
Disease: Abnormality of the philtrum
Abnormality of the philtrum 		phenotype Finding 6 0.100 None 0
CUI: C0392005
Disease: Bilateral cleft lip
Bilateral cleft lip 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Congenital Abnormality 8 1 0.100 None 0
CUI: C1844830
Disease: CLEFT PALATE, X-LINKED
CLEFT PALATE, X-LINKED 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases Disease or Syndrome 9 4 0.010 None 1.000 1 2004 2004
CUI: C4552482
Disease: CSSSI
CSSSI 		disease Disease or Syndrome 9 0.010 None 1.000 1 2014 2014
CUI: C4023573
Disease: Abnormal number of permanent teeth
Abnormal number of permanent teeth 		phenotype Anatomical Abnormality 9 0.100 None 0
CUI: C0679136
Disease: Low self-esteem
Low self-esteem 		phenotype Behavior and Behavior Mechanisms Finding 10 0.100 None 0
CUI: C1859363
Disease: Abnormality of dental eruption
Abnormality of dental eruption 		phenotype Finding 10 1 0.100 None 0
CUI: C2032780
Disease: Palate fistula
Palate fistula 		phenotype Finding 10 1 0.100 None 0
CUI: C4021881
Disease: Agenesis of lateral incisor
Agenesis of lateral incisor 		phenotype Anatomical Abnormality 10 0.100 None 0
CUI: C1843477
Disease: Epidermolysis Bullosa Simplex Superficialis
Epidermolysis Bullosa Simplex Superficialis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 11 0.010 None 1.000 1 2017 2017
CUI: C3553084
Disease: Bilateral cleft palate
Bilateral cleft palate 		phenotype Finding 11 1 0.100 None 0
CUI: C4025060
Disease: Peg-shaped maxillary lateral incisors
Peg-shaped maxillary lateral incisors 		phenotype Finding 11 0.100 None 0
CUI: C0263491
Disease: Pili Torti
Pili Torti 		phenotype Skin and Connective Tissue Diseases Finding 12 0.100 None 0