LMBR1, limb development membrane protein 1, 64327

N. diseases: 98; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0265559
Disease: Acheiropodia
Acheiropodia 		0.820 Biomarker disease CTD_human
CUI: C1868114
Disease: POLYDACTYLY, PREAXIAL II (disorder)
POLYDACTYLY, PREAXIAL II (disorder) 		0.730 CausalMutation disease CLINVAR
CUI: C1868114
Disease: POLYDACTYLY, PREAXIAL II (disorder)
POLYDACTYLY, PREAXIAL II (disorder) 		0.730 Biomarker disease CTD_human
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME 		0.700 Biomarker disease HPO
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME 		0.700 Biomarker disease CTD_human
CUI: C1861355
Disease: Syndactyly, Type IV
Syndactyly, Type IV 		0.610 Biomarker disease CTD_human
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.440 Biomarker disease HPO
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.440 Biomarker disease GENOMICS_ENGLAND
CUI: C1861098
Disease: Tibia, Hypoplasia of, with Polydactyly
Tibia, Hypoplasia of, with Polydactyly 		0.400 CausalMutation disease CLINVAR
CUI: C1851101
Disease: Laurin-Sandrow Syndrome, Segmental
Laurin-Sandrow Syndrome, Segmental 		0.300 Biomarker disease CTD_human
CUI: C1861099
Disease: Absence of tibia with polydactyly
Absence of tibia with polydactyly 		0.300 Biomarker disease CTD_human
CUI: C0241397
Disease: Triphalangeal thumb
Triphalangeal thumb 		0.120 Biomarker disease HPO
CUI: C0241397
Disease: Triphalangeal thumb
Triphalangeal thumb 		0.120 CausalMutation disease CLINVAR
CUI: C0039075
Disease: Syndactyly
Syndactyly 		0.110 Biomarker disease HPO
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		0.100 Biomarker disease HPO
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.100 Biomarker disease HPO
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.100 Biomarker group HPO
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		0.100 Biomarker disease HPO
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		0.100 Biomarker phenotype HPO
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		0.100 Biomarker phenotype HPO
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		0.100 Biomarker disease HPO
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		0.100 Biomarker disease HPO
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		0.100 Biomarker disease HPO
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		0.100 Biomarker disease HPO
CUI: C0265551
Disease: Dimelia
Dimelia 		0.100 Biomarker disease HPO