Search Ontology:
Human Disease

Smith-Lemli-Opitz syndrome

Term ID
DOID:14692
Synonyms
  • Rutledge lethal multiple congenital anomaly syndrome
  • Smith-Opitz-Inborn syndrome
Definition
References
  • GARD:5683
  • ICD10CM:E78.72
  • MESH:D019082
  • MIM:270400
  • NCI:C85071
  • SNOMEDCT_US_2023_03_01:43929004
  • UMLS_CUI:C0175694
Ontology
Human Disease   ( DOID:14692 )
Relationships
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Genes Involved
Zebrafish Models