Search Ontology:
Human Disease
Smith-Lemli-Opitz syndrome
- Term ID
- DOID:14692
- Synonyms
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- Rutledge lethal multiple congenital anomaly syndrome
- Smith-Opitz-Inborn syndrome
- Definition
- References
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- 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 )
- is a type of
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Genes Involved
Zebrafish Models