autosomal dominant intellectual developmental disorder 55

Summary
Synonym
  • autosomal dominant intellectual developmental disorder-55 with seizures
  • autosomal dominant mental retardation 55
Definition
An autosomal dominant intellectual developmental disorder that is characterized by onset of myoclonic seizures in the first years of life, global developmental delay, intellectual disability, speech delay and ataxic gait that has_material_basis_in heterozygous mutation in the NUS1 gene on chromosome 6q22.
Super Class
autosomal dominant intellectual developmental disorder
Disease Ontology
DOID:0080227
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
116150 NUS1 NUS1 dehydrodolichyl diphosphate synthase subunit
Displaying 1 entry
Gene ID Gene Symbol Description Source
52014 Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit
Displaying 1 entry
Gene ID Gene Symbol Description Source
436629 nus1 NUS1 dehydrodolichyl diphosphate synthase subunit
The Human Phenotype Ontology
Displaying entries 1 - 10 of 48 in total
HPO ID HPO Term
HP:0000648 Optic atrophy
HP:0000504 Abnormality of vision
HP:0000750 Delayed speech and language development
HP:0000348 High forehead
HP:0000708 Atypical behavior
HP:0001250 Seizure
HP:0000546 Retinal degeneration
HP:0000252 Microcephaly
HP:0000668 Hypodontia
HP:0001249 Intellectual disability
Displaying all 5 entries
Gene ID Gene Symbol Description
1759 DNM1 dynamin 1
523 ATP6V1A ATPase H+ transporting V1 subunit A
781 CACNA2D1 calcium voltage-gated channel auxiliary subunit alpha2delta 1
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
8867 SYNJ1 synaptojanin 1

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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