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Repository for lectin-assisted multimodality data
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Smith-Lemli-Opitz syndrome
Summary
- Synonym
-
- Rutledge lethal multiple congenital anomaly syndrome
- Smith-Opitz-Inborn syndrome
- Super Class
- lipid metabolism disorder
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001510 | Growth delay |
| HP:0001511 | Intrauterine growth retardation |
| HP:0001543 | Gastroschisis |
| HP:0001561 | Polyhydramnios |
| HP:0001600 | Abnormality of the larynx |
| HP:0001629 | Ventricular septal defect |
| HP:0001631 | Atrial septal defect |
| HP:0001643 | Patent ductus arteriosus |
| HP:0001830 | Postaxial foot polydactyly |
| HP:0001884 | Talipes calcaneovalgus |
