TP63, tumor protein p63, 8626

N. diseases: 816; N. variants: 64
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: C2363741
Disease: HIV-1 infection
HIV-1 infection
disease Disease or Syndrome 695 94 0.010 None 1.000 1 2002 2002
Cervical Intraepithelial Neoplasia Grade 2/3
disease Neoplastic Process 9 0.010 None 1.000 1 2011 2011
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
disease Congenital Abnormality 18 2 0.010 None 1.000 1 2019 2019
CUI: C3714796
Disease: Isolated somatotropin deficiency
Isolated somatotropin deficiency
disease Disease or Syndrome 168 27 0.110 None 1.000 1 2018 2018
CUI: C3805043
Disease: Vascular cognitive impairment
Vascular cognitive impairment
disease Disease or Syndrome 42 1 0.010 None 1.000 1 2018 2018
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD)
disease Disease or Syndrome 133 54 0.010 None 1.000 1 2004 2004
CUI: C4021813
Disease: Oral cleft
Oral cleft
disease Congenital Abnormality 85 28 0.100 None 1.000 1 1 2017 2017
CUI: C4021985
Disease: Germ cell neoplasia
Germ cell neoplasia
disease Neoplastic Process 22 0.010 None 1.000 1 2006 2006
CUI: C4049579
Disease: Keratin pearl
Keratin pearl
disease Neoplastic Process 5 0.010 None 1.000 1 2004 2004
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
disease Acquired Abnormality 120 1 0.100 None 0
CUI: C0239043
Disease: Difficulty chewing
Difficulty chewing
phenotype Finding 14 0.100 None 0
CUI: C0239174
Disease: Late tooth eruption
Late tooth eruption
phenotype Finding 139 4 0.100 None 0
CUI: C0239676
Disease: High forehead
High forehead
phenotype Finding 211 17 0.100 None 0
CUI: C0239801
Disease: Blonde hair
Blonde hair
phenotype Finding 13 0.100 None 0
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla
disease Congenital Abnormality 113 5 0.100 None 0
CUI: C0241633
Disease: Vaginal dryness
Vaginal dryness
phenotype Finding 1 0.100 None 0
CUI: C0277959
Disease: Coarse hair
Coarse hair
phenotype Finding 60 4 0.100 None 0
CUI: C0341059
Disease: Lip pit
Lip pit
disease Anatomical Abnormality 14 0.100 None 0
CUI: C0349588
Disease: Short stature
Short stature
phenotype Finding 1127 292 0.100 None 0
CUI: C0423757
Disease: Thin skin
Thin skin
phenotype Finding 77 4 0.100 None 0
CUI: C0423807
Disease: Overcurvature of nail
Overcurvature of nail
phenotype Finding 9 0.100 None 0
CUI: C0423867
Disease: Fine hair
Fine hair
phenotype Finding 69 1 0.100 None 0
CUI: C0425795
Disease: Absent nipple (finding)
Absent nipple (finding)
phenotype Finding 7 0.100 None 0
CUI: C0425913
Disease: Uterus absent (finding)
Uterus absent (finding)
phenotype Finding 10 1 0.100 None 0
CUI: C0426422
Disease: Narrow nose
Narrow nose
phenotype Finding 17 1 0.100 None 0