Search Ontology:
Human Disease

STAD syndrome

Term ID
DOID:0070699
Synonyms
  • skeletal dysplasia, tooth anomalies, and developmental delay syndrome
Definition
A syndrome characterized by a skeletal dysplasia consisting of advanced bone maturation, short and dysplastic bones, and disproportionate body measurements; facial dysmorphisms and dental anomalies; and neurodevelopmental delays ranging in severity from isolated fine motor delays to impaired intellectual development that has_material_basis_in heterozygous mutation in the PTBP1 gene on chromosome 19p13. https://pmc.ncbi.nlm.nih.gov/articles/PMC12618068/#sd
References
Ontology
Human Disease   ( DOID:0070699 )
Relationships
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Genes Involved
Zebrafish Models