OBO ID: DOID:0112285
Term Name: autosomal dominant spondyloepiphyseal dysplasia tarda Search Ontology:
Synonyms:
Definition: A spondyloepiphyseal dysplasia tarda that has_material_basis_in heterozygous mutation in a region of chromosome 12q13. (2)
References:
Ontology: Human Disease   ( DOID:0112285 )
Relationships
is a type of:
OTHER autosomal dominant spondyloepiphyseal dysplasia tarda PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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