Adams-Oliver syndrome

Summary
Synonym
  • Adams Oliver syndrome
Definition
A syndrome characterized by defects of the scalp (aplasia cutis congenita), abnormalities of the fingers, toes, arms and legs.
Super Class
syndrome
Disease Ontology
DOID:0060227
Mondo Disease Ontology
UMLS
ORDO
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 6 entries
Gene ID Gene Symbol Description Source
3516 RBPJ recombination signal binding protein for immunoglobulin kappa J region
4851 NOTCH1 notch receptor 1
54567 DLL4 delta like canonical Notch ligand 4
57514 ARHGAP31 Rho GTPase activating protein 31
57572 DOCK6 dedicator of cytokinesis 6
285203 EOGT EGF domain specific O-linked N-acetylglucosamine transferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
54485 Dll4 delta like canonical Notch ligand 4
The Human Phenotype Ontology
Displaying entries 31 - 40 of 58 in total
HPO ID HPO Term
HP:0002239 Gastrointestinal hemorrhage
HP:0002353 EEG abnormality
HP:0002612 Congenital hepatic fibrosis
HP:0002814 Abnormality of the lower limb
HP:0002817 Abnormality of the upper limb
HP:0004050 Absent hand
HP:0004935 Pulmonary artery atresia
HP:0005916 Abnormal metacarpal morphology
HP:0006101 Finger syndactyly
HP:0006970 Periventricular leukomalacia
Displaying 1 entry
Gene ID Gene Symbol Description
285203 EOGT EGF domain specific O-linked N-acetylglucosamine transferase

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.2.1

Last updated: April 7, 2025