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Transmembrane protein 199 congenital disorder of glycosylation

disorder
SNOMED 1208738002CUI C4225190

Overview

Transmembrane protein 199 congenital disorder of glycosylation is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormal protein N-linked glycosylation
Always present (100%)HP:0012347
Alanine aminotransferase increased
Always present (100%)HP:0031964
Copper accumulation in liver
Always present (100%)HP:0025321
Elevated alkaline phosphatase
Always present (100%)HP:0003155
Elevated circulating creatine phosphokinase
Always present (100%)HP:0003236
Elevated serum aspartate aminotransferase
Always present (100%)HP:0031956
Fatty liver
Always present (100%)HP:0001397
Hypoceruloplasminemia
Always present (100%)HP:0010837
Reduced serum copper
Always present (100%)HP:0011967
Subclinical abnormal liver function tests
Always present (100%)HP:0002910
Type II transferrin isoform profile
Always present (100%)HP:0012301
Elevated serum cholesterol
Very frequent (80-99%)HP:0003124
Increased plasma LDL levels
Very frequent (80-99%)HP:0003141
Abnormal protein O-linked glycosylation
Frequent (30-79%)HP:0012358
Enlarged liver
Frequent (30-79%)HP:0002240
Liver fibrosis
Frequent (30-79%)HP:0001395
Central hypotonia
Occasional (5-29%)HP:0001252
Mental and motor retardation
Occasional (5-29%)HP:0001263
Liver dysfunction, mild
HP:0001410

Quick Facts

SNOMED CT
1208738002
UMLS CUI
C4225190
Fully Specified Name
Transmembrane protein 199 congenital disorder of glycosylation (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
19
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.

Transmembrane protein 199 congenital disorder of glycosylation — Symptoms, Testing & Specialists | Healos | Ltrl