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Ontology Browser

Term:
Autosomal Dominant Craniometaphyseal Dysplasia (DOID:9007172)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
Autosomal Dominant Craniometaphyseal Dysplasia  
Autosomal Recessive Craniometaphyseal Dysplasia  
Schwartz-Lelek Syndrome  

Synonyms
Exact Synonyms: CMD ;   CMDD ;   CMDJ ;   Craniometaphyseal dysplasia Jackson type ;   Craniometaphyseal dysplasia dominant type
Primary IDs: MESH:C565145
Alternate IDs: OMIM:123000 ;   RDO:0013871

paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.