Smith-Lemli-Opitz syndrome

Summary
Synonym
  • Rutledge lethal multiple congenital anomaly syndrome
  • Smith-Opitz-Inborn syndrome
Super Class
lipid metabolism disorder
Disease Ontology
DOID:14692
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1717 DHCR7 7-dehydrocholesterol reductase
The Human Phenotype Ontology
Displaying entries 91 - 100 of 180 in total
HPO ID HPO Term
HP:0008056 Aplasia/Hypoplasia affecting the eye
HP:0008665 Clitoral hypertrophy
HP:0008678 Renal hypoplasia/aplasia
HP:0008736 Hypoplasia of penis
HP:0008872 Feeding difficulties in infancy
HP:0008905 Rhizomelia
HP:0009465 Ulnar deviation of finger
HP:0009623 Proximal placement of thumb
HP:0009804 Tooth agenesis
HP:0010297 Bifid tongue
Displaying 1 entry
Gene ID Gene Symbol Description
1717 DHCR7 7-dehydrocholesterol reductase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024