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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:oligodactyly
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Accession:MP:0000565 term browser browse the term
Definition:congenital condition in which some digits or parts of digits are missing
Synonyms:exact_synonym: hypodactyly
 alt_id: MP:0000563


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oligodactyly term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cntrob centrobin, centriole duplication and spindle assembly protein IAGP DNA:insertion:intron 10 (rat) RGD PMID:19710508 RGD:150521555 NCBI chr10:54,022,523...54,047,793
Ensembl chr10:54,022,852...54,044,849 		JBrowse link
G Cntrobhd centrobin, centriole duplication and spindle assembly protein; hypodacty mutant IAGP DNA:insertion:intron 10 (rat) RGD PMID:19710508 RGD:150521555
Term paths to the root
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Term Annotations click to browse term
  mammalian phenotype 5402
    limbs/digits/tail phenotype 76
      abnormal limb morphology 67
        abnormal autopod morphology 18
          abnormal digit morphology 11
            oligodactyly 2
              forelimb oligodactyly 0
              hindlimb oligodactyly + 0
paths to the root