WNT10B, Wnt family member 10B, 7480

N. diseases: 90; N. variants: 23
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2749665
Disease: SPLIT-HAND/FOOT MALFORMATION 6 (disorder)
SPLIT-HAND/FOOT MALFORMATION 6 (disorder) 		0.700 Biomarker disease CTD_human
CUI: C2749665
Disease: SPLIT-HAND/FOOT MALFORMATION 6 (disorder)
SPLIT-HAND/FOOT MALFORMATION 6 (disorder) 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C4310730
Disease: TOOTH AGENESIS, SELECTIVE, 8
TOOTH AGENESIS, SELECTIVE, 8 		0.600 Biomarker disease CTD_human
CUI: C4310730
Disease: TOOTH AGENESIS, SELECTIVE, 8
TOOTH AGENESIS, SELECTIVE, 8 		0.600 CausalMutation disease CLINVAR
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.420 Biomarker disease HPO
CUI: C4082304
Disease: Oligodontia
Oligodontia 		0.420 Biomarker disease HPO
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.110 GeneticVariation disease CLINVAR
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		0.110 Biomarker disease HPO
CUI: C0003076
Disease: Aniridia
Aniridia 		0.100 Biomarker disease HPO
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		0.100 Biomarker disease HPO
CUI: C0025990
Disease: Micrognathism
Micrognathism 		0.100 Biomarker disease HPO
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		0.100 Biomarker disease HPO
CUI: C0221373
Disease: Claw hand
Claw hand 		0.100 Biomarker disease HPO
CUI: C0240310
Disease: Hypoplasia of the maxilla
Hypoplasia of the maxilla 		0.100 Biomarker disease HPO
CUI: C0265594
Disease: Congenital absence of hand
Congenital absence of hand 		0.100 Biomarker disease HPO
CUI: C0265660
Disease: Syndactyly of the toes
Syndactyly of the toes 		0.100 Biomarker disease HPO
CUI: C0426868
Disease: Absence of hand
Absence of hand 		0.100 Biomarker phenotype HPO
CUI: C0432028
Disease: Split foot
Split foot 		0.100 Biomarker disease HPO
CUI: C0728895
Disease: Absent finger
Absent finger 		0.100 Biomarker disease HPO
CUI: C1970308
Disease: Selective tooth agenesis
Selective tooth agenesis 		0.100 Biomarker phenotype HPO
CUI: C3887496
Disease: Oligodactyly
Oligodactyly 		0.100 Biomarker disease HPO
CUI: C4281601
Disease: Foot oligodactyly
Foot oligodactyly 		0.100 Biomarker phenotype HPO
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.050 AlteredExpression disease BEFREE In fresh tissues, all Wnt genes apart from Wnt10b were expressed in normal endometrium and endometrial carcinoma. 9099960 1997
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.350 Biomarker disease BEFREE These findings suggest that the WNT10B gene may be involved in human breast cancer, and show that there is differential expression of the WNT10B gene in benign and malignant disease. 9121776 1997
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.350 AlteredExpression disease BEFREE In contrast, using both methods, WNT10B expression was found to be elevated in 3 of 50 primary breast carcinomas. 9121776 1997