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MAMMALIAN PHENOTYPE - ANNOTATIONS

The Mouse Adult Gross Anatomy Ontology and Mammalian Phenotype Ontology are downloaded weekly from the Mouse Genome Informatics databases at Jackson Laboratories (ftp://ftp.informatics.jax.org/pub/reports/index.html). For more information about these ontologies, see the MGI Publications Page at http://www.informatics.jax.org/mgihome/other/publications.shtml.

Term:alopecia
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Accession:MP:0000414 term browser browse the term
Definition:absence of hair due to loss of hair; not in reference to primary genetic hairlessness but may be due to dietary, stress or secondary to immune condition
Synonyms:exact_synonym: baldness;   hair loss;   loss of hair
 narrow_synonym: frontal fibrosing alopecia
 broad_synonym: absence of hair;   absence of hair shaft;   absent hair shaft;   no hair shaft
 related_synonym: hairless
 xref: EFO:0009855



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alopecia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Aire autoimmune regulator IMP RGD PMID:29959280 RGD:38599145 NCBI chr20:10,636,058...10,651,060
Ensembl chr20:10,636,123...10,651,060
JBrowse link
G Aireem1Ang autoimmune regulator; ZFN induced mutant1, Ang IMP RGD PMID:29959280 RGD:38599145
G Dsg4 desmoglein 4 IMP RGD PMID:15606503 RGD:150521560 NCBI chr18:11,720,844...11,757,927
Ensembl chr18:11,720,975...11,756,234
JBrowse link
G Dsg4hr desmoglein 4; hairless mutant IMP RGD PMID:15606503 RGD:150521560
G Gla galactosidase, alpha IMP RGD PMID:29979634 RGD:401976416 NCBI chr  X:97,769,227...97,780,646
Ensembl chr  X:97,768,996...97,780,664
JBrowse link
G Glaem2Mcwi galactosidase, alpha; CRISPR/Cas9 system induced mutant 2, Medical College of Wisconsin IMP RGD PMID:29979634 RGD:401976416
G Vdr vitamin D receptor IMP RGD PMID:32231239 RGD:32716373 NCBI chr 7:128,987,981...129,037,677
Ensembl chr 7:128,987,981...129,037,677
JBrowse link
G Vdrem2Thka vitamin D receptor; CRISPR/Cas9 induced mutant 2, Thka IMP RGD PMID:32231239 RGD:32716373

Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5415
    integument phenotype 171
      abnormal skin adnexa morphology 169
        abnormal coat/ hair morphology 63
          abnormal coat appearance 63
            abnormal hair growth 29
              alopecia 13
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