Simpson-Golabi-Behmel syndrome type 1

Summary
Synonym
  • DGSX Golabi-Rosen syndrome
  • Golabi-Rosen syndrome
  • SGB syndrome
  • Sara Angers syndrome
  • Simpson dysmorphia syndrome
  • X-linked dysplasia gigantism syndrome
  • bulldog syndrome
Definition
A syndrome characterized by pre- and postnatal overgrowth and craniofacial, skeletal, cardiac and renal abnormalities and has_material_basis_in mutation in the gene encoding glypican-3 (GPC3) on chromosome Xq26.
Super Class
X-linked recessive disease syndrome
External Links
Disease Ontology
DOID:0060248
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 10 entries
Gene ID Gene Symbol Description Source
960 CD44 CD44 molecule (IN blood group)
2262 GPC5 glypican 5
2719 GPC3 glypican 3
2817 GPC1 glypican 1
3251 HPRT1 hypoxanthine phosphoribosyltransferase 1
5277 PIGA phosphatidylinositol glycan anchor biosynthesis class A
6517 SLC2A4 solute carrier family 2 member 4
10082 GPC6 glypican 6
10135 NAMPT nicotinamide phosphoribosyltransferase
79709 COLGALT1 collagen beta(1-O)galactosyltransferase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
39013 dally division abnormally delayed
The Human Phenotype Ontology
Displaying entries 71 - 80 of 138 in total
HPO ID HPO Term
HP:0006101 Finger syndactyly
HP:0008736 Hypoplasia of penis
HP:0009536 Short 2nd finger
HP:0010318 Aplasia/Hypoplasia of the abdominal wall musculature
HP:0011039 Abnormal helix morphology
HP:0011304 Broad thumb
HP:0011710 Bundle branch block
HP:0030680 Abnormal cardiovascular system morphology
HP:0100490 Camptodactyly of finger
HP:0000105 Enlarged kidney
Displaying 1 entry
Gene ID Gene Symbol Description
2719 GPC3 glypican 3

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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: August 19, 2024