LPAR6, lysophosphatidic acid receptor 6, 10161

N. diseases: 47; N. variants: 10
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: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
disease Skin and Connective Tissue Diseases Disease or Syndrome 13 8 0.610 strong 1.000 4 7 2008 2014
CUI: C1854310
Disease: Hypotrichosis simplex
Hypotrichosis simplex
disease Skin and Connective Tissue Diseases Disease or Syndrome 37 5 0.510 None 1.000 3 2008 2009
CUI: C0020678
Disease: Hypotrichosis
Hypotrichosis
disease Skin and Connective Tissue Diseases Disease or Syndrome 69 2 0.500 None 1.000 13 2008 2019
CUI: C0343073
Disease: Wooly hair
Wooly hair
phenotype Skin and Connective Tissue Diseases Finding 19 0.400 None 1.000 1 2011 2011
CUI: C0345427
Disease: Woolly hair, congenital
Woolly hair, congenital
disease Skin and Connective Tissue Diseases Congenital Abnormality 5 0.300 None 1.000 1 2011 2011
CUI: C0002170
Disease: Alopecia
Alopecia
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 491 375 0.130 None 1.000 3 2009 2015
CUI: C1836672
Disease: Total Hypotrichosis, Mari type
Total Hypotrichosis, Mari type
disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Disease or Syndrome 27 4 0.100 None 1.000 10 2007 2013
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair
phenotype Finding 35 1 0.100 None 0
CUI: C0277959
Disease: Coarse hair
Coarse hair
phenotype Finding 60 4 0.100 None 0
CUI: C0423867
Disease: Fine hair
Fine hair
phenotype Finding 69 1 0.100 None 0
CUI: C1843300
Disease: Sparse eyelashes
Sparse eyelashes
phenotype Finding 60 4 0.100 None 0
WOOLLY HAIR, AUTOSOMAL RECESSIVE 1, WITH OR WITHOUT HYPOTRICHOSIS
disease Disease or Syndrome 2 1 0.100 None 0 1
CUI: C1849221
Disease: Fair hair
Fair hair
phenotype Finding 17 5 0.100 None 0
CUI: C1857206
Disease: Sparse lateral eyebrow
Sparse lateral eyebrow
phenotype Finding 20 0.100 None 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair
phenotype Finding 57 0.100 None 0
CUI: C1873509
Disease: Hypotrichosis of the scalp
Hypotrichosis of the scalp
phenotype Finding 12 1 0.100 None 0
CUI: C4282407
Disease: Sparse and thin eyebrow
Sparse and thin eyebrow
phenotype Finding 68 8 0.100 None 0
CUI: C0263490
Disease: Brittle hair
Brittle hair
disease Disease or Syndrome 45 1 0.100 None 0
CUI: C0239801
Disease: Blonde hair
Blonde hair
phenotype Finding 13 0.100 None 0
CUI: C0221228
Disease: Comedone
Comedone
disease Skin and Connective Tissue Diseases Disease or Syndrome 53 0.100 None 0
CUI: C3278401
Disease: Hypopigmentation of hair
Hypopigmentation of hair
phenotype Finding 23 1 0.100 None 0
CUI: C0154936
Disease: Pupillary abnormality
Pupillary abnormality
phenotype Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Finding 18 1 0.100 None 0
CUI: C0086543
Disease: Cataract
Cataract
disease Eye Diseases Acquired Abnormality 878 124 0.100 None 0
CUI: C0038379
Disease: Strabismus
Strabismus
disease Eye Diseases; Nervous System Diseases Disease or Syndrome 716 89 0.100 None 0
CUI: C0035300
Disease: Abnormal retinal morphology
Abnormal retinal morphology
phenotype Eye Diseases Finding 13 8 0.100 None 0