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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:abnormal cranial synchondrosis
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Accession:MP:0030443 term browser browse the term
Definition:any anomaly in the development of cartilaginous joints or growth centers between bones of the skull base by the formation of hyaline cartilage which is abundant during the growth phase and ultimately ossifies during skeletal maturation; synchondroses are composed of mirror-image growth plates with a central resting zone, proliferative zones, and hypertrophic zones on both sides; in mouse, there are two synchondroses in the midline cranial base, the sphenooccipital and presphenoidal synchondroses
Synonyms:exact_synonym: abnormal cranial synchondroses


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Path 1
Term Annotations click to browse term
  mammalian phenotype 5374
    skeleton phenotype 434
      abnormal skeleton morphology 339
        abnormal cartilage morphology 18
          abnormal cartilage development 7
            abnormal synchondrosis 0
              abnormal cranial synchondrosis 0
                abnormal presphenoid synchondrosis + 0
                abnormal sphenooccipital synchondrosis + 0
                premature cranial synchondrosis closure + 0
Path 2
Term Annotations click to browse term
  mammalian phenotype 5374
    skeleton phenotype 434
      abnormal skeleton morphology 339
        abnormal axial skeleton morphology 43
          abnormal craniofacial bone morphology 37
            abnormal cranium morphology 36
              abnormal cranial cartilage morphology 0
                abnormal cranial cartilage development 0
                  abnormal cranial synchondrosis 0
                    abnormal presphenoid synchondrosis + 0
                    abnormal sphenooccipital synchondrosis + 0
                    premature cranial synchondrosis closure + 0
paths to the root