Cleidocranial Dysplasia
flowchart AA["Associated Authors (0)"] C[Cleidocranial Dysplasia] BC["Broader Concepts (1)"] NC["Narrower Concepts (0)"] C== skos:broader ==>BC NC== skos:broader ==>C AA== dcterms:relation ==>C click BC "#broader-concepts" click NC "#narrower-concepts" click AA "#associated-authors" NI["add incoming edge"] NO["add outgoing edge"] NI-- ? -->C C-- ? -->NO click NI "#add-incoming-edge" click NO "#add-outgoing-edge" style NI stroke-width:2px,stroke-dasharray: 5 5 style NO stroke-width:2px,stroke-dasharray: 5 5
- Wikidata
- https://www.wikidata.org/wiki/Q781618
- OpenAlex ID
- https://openalex.org/C2908903051 (API record)
- OpenAlex Description
- osteochondrodysplasia that has material basis in mutations in the RUNX2 gene which results in undeveloped or absent located in clavicle along with delayed closing of fontanels in the located in skull
- OpenAlex Level [?]
- 3
Broader Concepts
Narrower Concepts
Associated Authors
Add Incoming Edge
Login via ORCiD to contribute.
Add Outgoing Edge
Login via ORCiD to contribute.