Yunis-Varon syndrome

Summary
Synonym
  • cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia
  • cleidocranial dysplasia-micrognathia-absent thumbs syndrome
Definition
A syndrome characterized by skeletal defects, including cleidocranial dysplasia and digital anomalies, and severe neurologic involvement with neuronal loss. Enlarged cytoplasmic vacuoles are found in neurons, muscle, and cartilage. It is usually lethal in infancy and has_material_basis_in homozygous or compound heterozygous mutation in the FIG4 gene on chromosome 6q21.
Super Class
autosomal recessive disease syndrome
Disease Ontology
DOID:0060589
Mondo Disease Ontology
MeSH
UMLS
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
9896 FIG4 FIG4 phosphoinositide 5-phosphatase
Displaying 1 entry
Gene ID Gene Symbol Description Source
33658 FIG4 FIG4 phosphoinositide 5-phosphatase
Displaying 1 entry
Gene ID Gene Symbol Description Source
855392 FIG4 phosphatidylinositol-3,5-bisphosphate 5-phosphatase
The Human Phenotype Ontology
Displaying entries 1 - 10 of 150 in total
HPO ID HPO Term
HP:0000028 Cryptorchidism
HP:0000047 Hypospadias
HP:0000054 Micropenis
HP:0000059 Hypoplastic labia majora
HP:0000162 Glossoptosis
HP:0000188 Short upper lip
HP:0000216 Broad secondary alveolar ridge
HP:0000233 Thin vermilion border
HP:0000238 Hydrocephalus
HP:0000268 Dolichocephaly
Displaying 1 entry
Gene ID Gene Symbol Description
9896 FIG4 FIG4 phosphoinositide 5-phosphatase

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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