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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/09/2024 MGI 6.23