TACR3, tachykinin receptor 3, 6870

N. diseases: 147; 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: C3553844
Disease: HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA 		disease Disease or Syndrome 1 7 0.900 strong 1.000 9 7 2007 2014
CUI: C0005890
Disease: Body Height
Body Height 		phenotype Organism Attribute 1903 3972 0.100 None 1.000 2 2 2019 2019
CUI: C0342381
Disease: Idiopathic growth hormone deficiency
Idiopathic growth hormone deficiency 		disease Disease or Syndrome 10 0.200 None 1.000 2 2007 2012
CUI: C2874188
Disease: Isolated deficiency of pituitary hormone
Isolated deficiency of pituitary hormone 		disease Disease or Syndrome 8 0.200 None 1.000 2 2007 2012
CUI: C2874189
Disease: Necrosis of pituitary gland (postpartum)
Necrosis of pituitary gland (postpartum) 		phenotype Pathologic Function 8 0.200 None 1.000 2 2007 2012
CUI: C2874190
Disease: Pituitary short stature
Pituitary short stature 		disease Disease or Syndrome 8 0.200 None 1.000 2 2007 2012
CUI: C4552011
Disease: Gonadotropin deficiency
Gonadotropin deficiency 		disease Disease or Syndrome 26 0.020 None 1.000 2 2009 2017
CUI: C0028081
Disease: Night sweats
Night sweats 		phenotype Sign or Symptom 17 0.010 None 1.000 1 2017 2017
CUI: C0342538
Disease: Constitutional delay of growth and puberty
Constitutional delay of growth and puberty 		disease Disease or Syndrome 16 7 0.010 None 1.000 1 1 2011 2011
CUI: C1278797
Disease: Postnatal infection
Postnatal infection 		disease Disease or Syndrome 5 0.010 None 1.000 1 2012 2012
CUI: C1402294
Disease: Primary Lesion
Primary Lesion 		phenotype Disease or Syndrome 71 8 0.010 None 1.000 1 2010 2010
CUI: C1519666
Disease: Tumor-Associated Vasculature
Tumor-Associated Vasculature 		disease Acquired Abnormality 84 0.010 None 1.000 1 2017 2017
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2009 2009
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		disease Acquired Abnormality 120 1 0.100 None 0
CUI: C0240701
Disease: Small penis
Small penis 		phenotype Finding 11 2 0.100 None 0
CUI: C0241355
Disease: Small testicle
Small testicle 		phenotype Finding 129 0.100 None 0
CUI: C0520927
Disease: Decreased fertility
Decreased fertility 		phenotype Finding 50 0.100 None 0
CUI: C0541764
Disease: Delayed bone age
Delayed bone age 		phenotype Finding 295 14 0.100 None 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		phenotype Finding 96 19 0.100 None 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		phenotype Finding 44 6 0.100 None 0
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge 		phenotype Finding 426 39 0.100 None 0
CUI: C1846228
Disease: Absence of pubertal development
Absence of pubertal development 		phenotype Finding 24 0.100 None 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair 		phenotype Finding 57 0.100 None 0
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype Finding 779 0.100 None 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		phenotype Finding 76 2 0.100 None 0