Metadata | |
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ID | DOID:0111533 |
Name | gnathodiaphyseal dysplasia |
Definition | An osteochondrodysplasia characterized by cementoosseous lesions of the jawbones, bone fragility, bowing/cortical thickening of tubular bones, and diaphyseal sclerosis of long bones that has_material_basis_in heterozygous mutation in the ANO5 gene on chromosome 11p14.3. https://ghr.nlm.nih.gov/condition/gnathodiaphyseal-dysplasia, https://www.ncbi.nlm.nih.gov/pubmed/15124103, https://www.ncbi.nlm.nih.gov/pubmed/23047743 |
Xrefs |
SNOMEDCT_US_2023_03_01:715568002 |
Subsets |
DO_rare_slim |
Synonyms |
GDD [EXACT] gnathodiaphyseal sclerosis [EXACT] Levin syndrome 2 [EXACT] osteogenesis imperfecta with unusual skeletal lesions [EXACT] osteogenesis imperfecta, Levin type [EXACT] |
Parent Relationships |