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 151 - 160 of 180 in total
HPO ID HPO Term
HP:0001765 Hammertoe
HP:0001831 Short toe
HP:0001840 Metatarsus adductus
HP:0001845 Overlapping toe
HP:0002013 Vomiting
HP:0002019 Constipation
HP:0002033 Poor suck
HP:0002079 Hypoplasia of the corpus callosum
HP:0002240 Hepatomegaly
HP:0002283 Global brain atrophy
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