ONTOLOGY REPORT - ANNOTATIONS


Term:alopecia
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Accession:DOID:987 term browser browse the term
Definition:Absence of hair from areas where it is normally present.
Synonyms:exact_synonym: AGA1;   Alopecia, Androgenetic, 1;   Baldness;   Female Pattern Baldness;   Hair Loss;   Hair Losses;   Male Pattern Alopecia;   alopecia cicatrisata;   alopecia cicatrisatas;   generic alopecia;   male pattern baldness;   pattern baldness;   pseudopelade
 narrow_synonym: AGA BALDNESS, MALE PATTERN;   ANDROGENETIC ALOPECIA;   Alopecia, color mutant;   MPB
 primary_id: MESH:D000505
 alt_id: OMIA:000030;   OMIA:000031;   OMIM:109200;   OMIM:300042;   RDO:0000400
 xref: OMIM:PS203655
For additional species annotation, visit the Alliance of Genome Resources.


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alopecia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcc2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2 JBrowse link 19 43,782,308 43,838,332 RGD:11554173
G Ar androgen receptor JBrowse link X 98,148,757 98,323,218 RGD:11554173
G Bdnf brain derived neurotrophic factor JBrowse link 2 109,674,700 109,727,043 RGD:8657081
G Brd4 bromodomain containing 4 JBrowse link 17 32,196,272 32,284,722 RGD:11554173
G Col7a1 collagen, type VII, alpha 1 JBrowse link 9 108,953,575 108,984,876 RGD:8554872
G Crh corticotropin releasing hormone JBrowse link 3 19,693,401 19,695,396 RGD:11554173
G Esr2 estrogen receptor 2 (beta) JBrowse link 12 76,120,419 76,177,259 RGD:8694094
RGD:8694095
G Far2 fatty acyl CoA reductase 2 JBrowse link 6 148,047,011 148,182,760 RGD:13592920
G Foxn1 forkhead box N1 JBrowse link 11 78,357,577 78,387,654 RGD:1599846
G H2-Q4 histocompatibility 2, Q region locus 4 JBrowse link 17 35,379,617 35,384,674 RGD:7387278
G Hr lysine demethylase and nuclear receptor corepressor JBrowse link 14 70,554,056 70,573,548 RGD:1599575
RGD:11554173
G Igf1 insulin-like growth factor 1 JBrowse link 10 87,858,265 87,937,047 RGD:8549462
RGD:8549500
G Mfn2 mitofusin 2 JBrowse link 4 147,873,586 147,904,909 RGD:8554872
G Mthfr methylenetetrahydrofolate reductase JBrowse link 4 148,038,317 148,059,565 RGD:11554173
G Parp1 poly (ADP-ribose) polymerase family, member 1 JBrowse link 1 180,568,975 180,601,254 RGD:11554173
G Plcd1 phospholipase C, delta 1 JBrowse link 9 119,071,527 119,093,592 RGD:1302551
G Srd5a2 steroid 5 alpha-reductase 2 JBrowse link 17 74,017,706 74,047,916 RGD:11554173
G Supv3l1 suppressor of var1, 3-like 1 (S. cerevisiae) JBrowse link 10 62,429,329 62,451,295 RGD:11554173
G Tnfrsf10b tumor necrosis factor receptor superfamily, member 10b JBrowse link 14 69,767,472 69,784,411 RGD:11554173
G Tpmt thiopurine methyltransferase JBrowse link 13 47,021,987 47,043,338 RGD:11038725
G Vdr vitamin D (1,25-dihydroxyvitamin D3) receptor JBrowse link 15 97,854,427 97,908,296 RGD:8157637
RGD:11554173
G Zdhhc13 zinc finger, DHHC domain containing 13 JBrowse link 7 48,789,003 48,827,437 RGD:11554173
G Zfp36 zinc finger protein 36 JBrowse link 7 28,376,784 28,379,228 RGD:11554173
alopecia areata term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G 9230019H11Rik RIKEN cDNA 9230019H11 gene JBrowse link 10 3,119,812 3,129,546 RGD:11554173
G Ctla4 cytotoxic T-lymphocyte-associated protein 4 JBrowse link 1 60,909,025 60,915,832 RGD:7411701
RGD:11554173
G Cxcl10 chemokine (C-X-C motif) ligand 10 JBrowse link 5 92,346,638 92,348,889 RGD:11554173
G Cxcl9 chemokine (C-X-C motif) ligand 9 JBrowse link 5 92,321,331 92,328,079 RGD:11554173
G Cxcr3 chemokine (C-X-C motif) receptor 3 JBrowse link X 101,731,535 101,734,147 RGD:11554173
G Dnmt1 DNA methyltransferase (cytosine-5) 1 JBrowse link 9 20,907,206 20,959,888 RGD:9587460
G Ehmt2 euchromatic histone lysine N-methyltransferase 2 JBrowse link 17 34,898,466 34,914,051 RGD:9587460
G H2-Aa histocompatibility 2, class II antigen A, alpha JBrowse link 17 34,282,751 34,287,771 RGD:8547568
G H2-Ab1 histocompatibility 2, class II antigen A, beta 1 JBrowse link 17 34,263,227 34,269,418 RGD:8547568
G Hdac1 histone deacetylase 1 JBrowse link 4 129,516,104 129,542,646 RGD:9587460
G Hdac2 histone deacetylase 2 JBrowse link 10 36,974,544 37,001,889 RGD:9587460
G Hdac7 histone deacetylase 7 JBrowse link 15 97,792,664 97,844,502 RGD:9587460
G Ikzf4 IKAROS family zinc finger 4 JBrowse link 10 128,630,839 128,669,809 RGD:11554173
G Il18 interleukin 18 JBrowse link 9 50,554,705 50,581,841 RGD:8655875
G Il1rn interleukin 1 receptor antagonist JBrowse link 2 24,336,860 24,351,491 RGD:6909137
G Il2 interleukin 2 JBrowse link 3 37,120,713 37,125,954 RGD:8663449
RGD:8663450
G Il2ra interleukin 2 receptor, alpha chain JBrowse link 2 11,642,792 11,693,194 RGD:11554173
G Kdm1a lysine (K)-specific demethylase 1A JBrowse link 4 136,550,533 136,602,790 RGD:9587460
G Kdm4a lysine (K)-specific demethylase 4A JBrowse link 4 118,136,957 118,180,043 RGD:9587460
G Kdm4b lysine (K)-specific demethylase 4B JBrowse link 17 56,326,033 56,403,769 RGD:9587460
G Kdm4c lysine (K)-specific demethylase 4C JBrowse link 4 74,242,497 74,405,864 RGD:9587460
G Kdm5a lysine (K)-specific demethylase 5A JBrowse link 6 120,364,099 120,444,574 RGD:9587460
G Notch4 notch 4 JBrowse link 17 34,564,277 34,588,543 RGD:6480681
G Prdx5 peroxiredoxin 5 JBrowse link 19 6,906,819 6,909,645 RGD:11554173
G Ptpn22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid) JBrowse link 3 103,856,802 103,912,252 RGD:6484734
G Stx17 syntaxin 17 JBrowse link 4 48,124,915 48,186,507 RGD:11554173
G Trps1 transcriptional repressor GATA binding 1 JBrowse link 15 50,654,757 50,890,750 RGD:8554872
Alopecia Congenita Keratosis Palmoplantaris term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gja1 gap junction protein, alpha 1 JBrowse link 10 56,377,300 56,390,419 RGD:8554872
alopecia universalis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hr lysine demethylase and nuclear receptor corepressor JBrowse link 14 70,554,056 70,573,548 RGD:7240710
RGD:8554872
RGD:13592920
G Il4 interleukin 4 JBrowse link 11 53,612,460 53,618,665 RGD:7829773
Alopecia, Neurologic Defects, and Endocrinopathy Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rbm28 RNA binding motif protein 28 JBrowse link 6 29,123,573 29,164,724 RGD:7240710
RGD:8554872
Alopecia-Mental Retardation Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ahsg alpha-2-HS-glycoprotein JBrowse link 16 22,892,015 22,899,451 RGD:8554872
RGD:7240710
atrichia with papular lesions term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Hr lysine demethylase and nuclear receptor corepressor JBrowse link 14 70,554,056 70,573,548 RGD:7240710
RGD:8554872
RGD:13592920
G Odc1 ornithine decarboxylase, structural 1 JBrowse link 12 17,544,867 17,551,502 RGD:13592920
Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sash1 SAM and SH3 domain containing 1 JBrowse link 10 8,722,217 9,027,745 RGD:7240710
RGD:8554872
Central Centrifugal Cicatricial Alopecia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Padi3 peptidyl arginine deiminase, type III JBrowse link 4 140,785,369 140,810,648 RGD:8554872
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Htra1 HtrA serine peptidase 1 JBrowse link 7 130,936,203 130,985,658 RGD:7240710
RGD:8554872
Cutaneous Telangiectasia and Cancer Syndrome, Familial term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Atr ataxia telangiectasia and Rad3 related JBrowse link 9 95,857,597 95,953,217 RGD:7240710
RGD:8554872
Dermatopathia Pigmentosa Reticularis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Krt14 keratin 14 JBrowse link 11 100,203,162 100,207,510 RGD:7240710
RGD:8554872
Frontonasal Dysplasia 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Alx4 aristaless-like homeobox 4 JBrowse link 2 93,642,434 93,681,341 RGD:7240710
RGD:8554872
Glomerulonephritis with Sparse Hair and Telangiectases term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Sox18 SRY (sex determining region Y)-box 18 JBrowse link 2 181,669,837 181,671,640 RGD:8554872
RGD:7240710
G Tcea2 transcription elongation factor A (SII), 2 JBrowse link 2 181,680,272 181,688,069 RGD:8554872
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Antxr1 anthrax toxin receptor 1 JBrowse link 6 87,133,853 87,335,809 RGD:9684854
RGD:8554872
RGD:7240710
hypotrichosis 7 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Liph lipase, member H JBrowse link 16 21,953,817 21,995,658 RGD:8554872
RGD:7240710
Ichthyosis Follicularis Atrichia Photophobia Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gjb2 gap junction protein, beta 2 JBrowse link 14 57,098,602 57,104,702 RGD:8554872
G Mbtps2 membrane-bound transcription factor peptidase, site 2 JBrowse link X 157,547,822 157,598,715 RGD:7240710
RGD:8554872
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Rin2 Ras and Rab interactor 2 JBrowse link 2 145,771,727 145,887,616 RGD:7240710
RGD:8554872
mandibulofacial dysostosis with alopecia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ednra endothelin receptor type A JBrowse link 8 77,663,029 77,724,452 RGD:8554872
RGD:13592920
RGD:7240710
Nisch syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cldn1 claudin 1 JBrowse link 16 26,356,645 26,371,839 RGD:7240710
RGD:11341732
RGD:8554872
Noonan Syndrome-Like Disorder with Loose Anagen Hair term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Shoc2 Shoc2, leucine rich repeat scaffold protein JBrowse link 19 53,944,232 54,033,280 RGD:8554872
Noonan Syndrome-Like Disorder with Loose Anagen Hair 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Shoc2 Shoc2, leucine rich repeat scaffold protein JBrowse link 19 53,944,232 54,033,280 RGD:7240710
RGD:8554872
Noonan Syndrome-Like Disorder with Loose Anagen Hair 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ppp1cb protein phosphatase 1 catalytic subunit beta JBrowse link 5 32,458,848 32,493,712 RGD:8554872
RGD:7240710
PALMOPLANTAR KERATODERMA AND CONGENITAL ALOPECIA 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Gja1 gap junction protein, alpha 1 JBrowse link 10 56,377,300 56,390,419 RGD:7240710
T-cell immunodeficiency, congenital alopecia, and nail dystrophy term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Foxn1 forkhead box N1 JBrowse link 11 78,357,577 78,387,654 RGD:7240710
RGD:8554872
RGD:13592920
Woodhouse Sakati Syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dcaf17 DDB1 and CUL4 associated factor 17 JBrowse link 2 71,055,742 71,116,414 RGD:7240710
RGD:8554872
G Mettl8 methyltransferase like 8 JBrowse link 2 70,964,558 71,055,643 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11832
    Pathological Conditions, Signs and Symptoms 6892
      Anatomical Pathological Conditions 1197
        alopecia 74
          Alopecia Congenita Keratosis Palmoplantaris + 1
          Alopecia Contractures Dwarfism Mental Retardation 0
          Alopecia Epilepsy Oligophrenia Syndrome of Moynahan 0
          Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia 0
          Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 0
          Alopecia, Hypogonadism, Extrapyramidal Disorder 0
          Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 1
          Alopecia-Mental Retardation Syndrome + 1
          Androgenetic Alopecia 2 0
          Androgenetic Alopecia 3 0
          Bullous Dystrophy, Hereditary Macular Type 0
          Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma 1
          Cataract, Alopecia, Sclerodactyly 0
          Central Centrifugal Cicatricial Alopecia 1
          Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 1
          Congenital Alopecia X-Linked 0
          Cutaneous Telangiectasia and Cancer Syndrome, Familial 1
          Dermatopathia Pigmentosa Reticularis 1
          Ectodermal Dysplasia Alopecia Preaxial Polydactyly 0
          Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 0
          Familial Focal Alopecia 0
          Follicular Hamartoma, Alopecia, Cystic Fibrosis 0
          Frontonasal Dysplasia 2 1
          Garret Tripp Syndrome 0
          Glomerulonephritis with Sparse Hair and Telangiectases 2
          Gomez Lopez Hernandez Syndrome 0
          Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy 1
          Hypergonadotropic Hypogonadism And Partial Alopecia 0
          Ichthyosis Follicularis Atrichia Photophobia Syndrome 2
          Jagell Holmgren Hofer Syndrome 0
          Johnson Neuroectodermal Syndrome 0
          Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant 0
          Kuster Majewski Hammerstein Syndrome 0
          Loose Anagen Hair Syndrome + 2
          Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 1
          Microcephaly Sparse Hair Mental Retardation Seizures 0
          Moloney Syndrome 0
          Nisch syndrome 1
          PARC Syndrome 0
          Patel Bixler Syndrome 0
          Perniola Krajewska Carnevale Syndrome 0
          Satoyoshi Syndrome 0
          Scholte Syndrome 0
          Slti Salem Syndrome 0
          T-cell immunodeficiency, congenital alopecia, and nail dystrophy 1
          Thumb Deformity and Alopecia 0
          Thumb Deformity, Alopecia, Pigmentation Anomaly 0
          Urban Schosser Spohn Syndrome 0
          Woodhouse Sakati Syndrome 2
          Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears 0
          alopecia areata + 27
          alopecia universalis + 2
          androgenic alopecia 0
          atrichia with papular lesions 2
          follicular mucinosis 0
          hypotrichosis 7 1
          mandibulofacial dysostosis with alopecia 1
          telogen effluvium 0
Path 2
Term Annotations click to browse term
  disease 11832
    disease of anatomical entity 11283
      nervous system disease 8564
        sensory system disease 4038
          skin disease 2129
            hair disease 212
              hypotrichosis 96
                alopecia 74
                  Alopecia Congenita Keratosis Palmoplantaris + 1
                  Alopecia Contractures Dwarfism Mental Retardation 0
                  Alopecia Epilepsy Oligophrenia Syndrome of Moynahan 0
                  Alopecia Universalis Congenita, XY Gonadal Dysgenesis, and Laryngomalacia 0
                  Alopecia, Epilepsy, Pyorrhea, Mental Subnormality 0
                  Alopecia, Hypogonadism, Extrapyramidal Disorder 0
                  Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 1
                  Alopecia-Mental Retardation Syndrome + 1
                  Androgenetic Alopecia 2 0
                  Androgenetic Alopecia 3 0
                  Bullous Dystrophy, Hereditary Macular Type 0
                  Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma 1
                  Cataract, Alopecia, Sclerodactyly 0
                  Central Centrifugal Cicatricial Alopecia 1
                  Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 1
                  Congenital Alopecia X-Linked 0
                  Cutaneous Telangiectasia and Cancer Syndrome, Familial 1
                  Dermatopathia Pigmentosa Reticularis 1
                  Ectodermal Dysplasia Alopecia Preaxial Polydactyly 0
                  Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet 0
                  Familial Focal Alopecia 0
                  Follicular Hamartoma, Alopecia, Cystic Fibrosis 0
                  Frontonasal Dysplasia 2 1
                  Garret Tripp Syndrome 0
                  Glomerulonephritis with Sparse Hair and Telangiectases 2
                  Gomez Lopez Hernandez Syndrome 0
                  Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy 1
                  Hypergonadotropic Hypogonadism And Partial Alopecia 0
                  Ichthyosis Follicularis Atrichia Photophobia Syndrome 2
                  Jagell Holmgren Hofer Syndrome 0
                  Johnson Neuroectodermal Syndrome 0
                  Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant 0
                  Kuster Majewski Hammerstein Syndrome 0
                  Loose Anagen Hair Syndrome + 2
                  Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 1
                  Microcephaly Sparse Hair Mental Retardation Seizures 0
                  Moloney Syndrome 0
                  Nisch syndrome 1
                  PARC Syndrome 0
                  Patel Bixler Syndrome 0
                  Perniola Krajewska Carnevale Syndrome 0
                  Satoyoshi Syndrome 0
                  Scholte Syndrome 0
                  Slti Salem Syndrome 0
                  T-cell immunodeficiency, congenital alopecia, and nail dystrophy 1
                  Thumb Deformity and Alopecia 0
                  Thumb Deformity, Alopecia, Pigmentation Anomaly 0
                  Urban Schosser Spohn Syndrome 0
                  Woodhouse Sakati Syndrome 2
                  Woolly Hair, Hypotrichosis, Everted Lower Lip and Outstanding Ears 0
                  alopecia areata + 27
                  alopecia universalis + 2
                  androgenic alopecia 0
                  atrichia with papular lesions 2
                  follicular mucinosis 0
                  hypotrichosis 7 1
                  mandibulofacial dysostosis with alopecia 1
                  telogen effluvium 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.