Search Ontology:
Human Disease
omodysplasia 2
- Term ID
- DOID:0080845
- Synonyms
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- Definition
- An omodysplasia that is characterized by shortened humeri, dislocated radial heads, shortened first metacarpals, craniofacial dysmorphism, and variable genitourinary anomalies and that has_material_basis_in heterozygous mutation in the FZD2 gene on chromosome 17q21. https://pubmed.ncbi.nlm.nih.gov/25759469/
- References
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- MESH:C567664
- MIM:164745
- SNOMEDCT_US_2023_03_01:725165009
- UMLS_CUI:C2750355
- Ontology
- Human Disease ( DOID:0080845 )
- is a type of
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Genes Involved
Zebrafish Models