LPAR6, lysophosphatidic acid receptor 6, 10161

N. diseases: 47; N. variants: 10
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8 		0.610 CausalMutation disease CLINVAR
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		0.500 Biomarker disease CTD_human
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis 		0.500 Biomarker disease HPO
CUI: C0343073
Disease: Wooly hair
Wooly hair 		0.400 Biomarker phenotype HPO
CUI: C0002170
Disease: Alopecia
Alopecia 		0.130 Biomarker disease HPO
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology 		0.100 Biomarker phenotype HPO
CUI: C0038379
Disease: Strabismus
Strabismus 		0.100 Biomarker disease HPO
CUI: C0086543
Disease: Cataract
Cataract 		0.100 Biomarker disease HPO
CUI: C0154936
Disease: Pupillary abnormality
Pupillary abnormality 		0.100 Biomarker phenotype HPO
CUI: C0221228
Disease: Comedone
Comedone 		0.100 Biomarker disease HPO
CUI: C0239801
Disease: Blonde hair
Blonde hair 		0.100 Biomarker phenotype HPO
CUI: C0263490
Disease: Brittle hair
Brittle hair 		0.100 Biomarker disease HPO
CUI: C0277959
Disease: Coarse hair
Coarse hair 		0.100 Biomarker phenotype HPO
CUI: C0423867
Disease: Fine hair
Fine hair 		0.100 Biomarker phenotype HPO
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair 		0.100 Biomarker phenotype HPO
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes 		0.100 Biomarker phenotype HPO
CUI: C1848435
Disease: WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS
WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS 		0.100 CausalMutation disease CLINVAR
CUI: C1849221
Disease: Fair hair
Fair hair 		0.100 Biomarker phenotype HPO
CUI: C1857206
Disease: Sparse lateral eyebrow
Sparse lateral eyebrow 		0.100 Biomarker phenotype HPO
CUI: C1862863
Disease: Sparse body hair
Sparse body hair 		0.100 Biomarker phenotype HPO
CUI: C1873509
Disease: Hypotrichosis of the scalp
Hypotrichosis of the scalp 		0.100 Biomarker phenotype HPO
CUI: C3278401
Disease: Hypopigmentation of hair
Hypopigmentation of hair 		0.100 Biomarker phenotype HPO
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow 		0.100 Biomarker phenotype HPO
CUI: C3502073
Disease: Woolly Hair, Autosomal Recessive
Woolly Hair, Autosomal Recessive 		0.070 GeneticVariation disease BEFREE Autosomal recessive woolly hair (ARWH) was recently determined to result from mutations in either the lipase H (LIPH) or the LPAR6 (P2RY5) gene. 23590372 2013
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.040 Biomarker group BEFREE P2RY5 is a gene encoded within intron 17 of RB1, a prototypic tumor suppressor gene whose expression is lost at a later stage of bladder carcinogenesis. 18475256 2008