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Glucose-6-phosphate transport defect

disorder
SNOMED 30102006CUI C0268146

Overview

By MedlinePlus, National Library of Medicine

Courtesy of the National Library of Medicine. Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Large spleen
Always present (100%)HP:0001744
Neutropoenia
Always present (100%)HP:0001875
Pancreatic fibrosis
Always present (100%)HP:0100732
Reduced hepatic glucose-6-phosphate translocase activity
Always present (100%)HP:6000201
Abdominal protuberance
Very frequent (80-99%)HP:0001538
Abnormal circulating enzyme concentration or activity
Very frequent (80-99%)HP:0012379
Decreased body height
Very frequent (80-99%)HP:0004322
Elevated serum cholesterol
Very frequent (80-99%)HP:0003124
Enlarged liver
Very frequent (80-99%)HP:0002240
Hyperlipidemia
Very frequent (80-99%)HP:0003077
Hyperuricaemia
Very frequent (80-99%)HP:0002149
Increased hepatic glycogen content
Very frequent (80-99%)HP:0006568
Increased triglycerides
Very frequent (80-99%)HP:0002155
Lacticacidosis
Very frequent (80-99%)HP:0003128
Low blood sugar
Very frequent (80-99%)HP:0001943
Poor growth
Very frequent (80-99%)HP:0001510
Abnormality of myeloid leukocytes
Frequent (30-79%)HP:0010974
Chronic neutropenia
Frequent (30-79%)HP:0410252
Deficient in vitamin D
Frequent (30-79%)HP:0100512
Enlarged kidney
Frequent (30-79%)HP:0000105
Fatty liver
Frequent (30-79%)HP:0001397
Hyperplasia of cheeks
Frequent (30-79%)HP:0000293
Menstrual irregularity
Frequent (30-79%)HP:0000858
No development of motor milestones
Frequent (30-79%)HP:0001270
Osteoporosis
Frequent (30-79%)HP:0000939
Pancreatitis
Frequent (30-79%)HP:0001733
Postnatal failure to thrive
Frequent (30-79%)HP:0001508
Psychomotor development deficiency
Frequent (30-79%)HP:0001263
Recurrent bacterial infections
Frequent (30-79%)HP:0002718
Round, full face
Frequent (30-79%)HP:0000311

Quick Facts

SNOMED CT
30102006
UMLS CUI
C0268146
Fully Specified Name
Glucose-6-phosphate transport defect (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.