Source: HPO

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C0029454
Disease: Osteopetrosis
Osteopetrosis 		disease 0.450 moderate 1.000 0 0 2001 2014
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		disease 0.200 None 1.000 0 0 2004 2019
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C0151825
Disease: Bone pain
Bone pain 		phenotype 0.110 None 1.000 0 0 2011 2011
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		group 0.110 None 1.000 0 0 2015 2015
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1856409
Disease: Dilation of lateral ventricles
Dilation of lateral ventricles 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1855841
Disease: Hypocalcemic seizures
Hypocalcemic seizures 		disease 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1855340
Disease: Bowing of the long bones
Bowing of the long bones 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1854301
Disease: Motor delay
Motor delay 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1833325
Disease: Thin bony cortex
Thin bony cortex 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1832451
Disease: Cranial hyperostosis
Cranial hyperostosis 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1390474
Disease: Increased susceptibility to fractures
Increased susceptibility to fractures 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1314665
Disease: Serum alkaline phosphatase raised
Serum alkaline phosphatase raised 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C0948585
Disease: Hydroxyprolinuria
Hydroxyprolinuria 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C1865903
Disease: Long-tract signs
Long-tract signs 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C4721411
Disease: Osteolysis
Osteolysis 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C4554063
Disease: Bone Pain, CTCAE 5.0
Bone Pain, CTCAE 5.0 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C4083076
Disease: Increased head circumference
Increased head circumference 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C4048270
Disease: Decreased antibody level in blood
Decreased antibody level in blood 		phenotype 0.100 None 0 0
Entrez Id: 8792
Gene Symbol: TNFRSF11A
TNFRSF11A 		TNF receptor superfamily member 11a 0.480 0.846 8.8E-03
CUI: C4021792
Disease: Abnormality of the clavicle
Abnormality of the clavicle 		disease 0.100 None 0 0