Ccd Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ccd
cleidocranial dysplasia
MGI:88291

24 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ccd/Ccd⁺ Shh^Dsh/Shh⁺ involves: 101 * C3H * C57BL * C57BL/10Rl * SEC	abnormal clavicle morphology	J:16170
	abnormal cranium morphology	J:16170
	abnormal hindlimb morphology	J:16170
	abnormal humerus morphology	J:16170
	abnormal interparietal bone morphology	J:16170
	abnormal ischium morphology	J:16170
	abnormal maxilla morphology	J:16170
	abnormal neurocranium morphology	J:16170
	abnormal orbit morphology	J:16170
	abnormal pectoral girdle bone morphology	J:16170
	abnormal pelvic girdle bone morphology	J:16170
	abnormal pubis morphology	J:16170
	abnormal scapula morphology	J:16170
	abnormal temporal bone squamous part morphology	J:16170
	abnormal ventral tubercle of atlas morphology	J:16170
	abnormal vertebrae morphology	J:16170
	abnormal xiphoid process morphology	J:16170
	absent deltoid tuberosity	J:16170
	absent nasal bone	J:16170
	brachydactyly	J:16170
	fusion of atlas and odontoid process	J:16170
	occipital bone foramen	J:16170
	premature death	J:16170
	syndactyly	J:16170

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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