Tryptophan malabsorption syndrome

disorder

SNOMED 59531002CUI C0268478

Overview

Tryptophan malabsorption syndrome 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.

Blue urine

Very frequent (80-99%)HP:0040317

Diarrhea

Frequent (30-79%)HP:0002014

Hypercalcemia

Frequent (30-79%)HP:0003072

Increased body weight

Frequent (30-79%)HP:0004324

Increased calcium level in kidney

Frequent (30-79%)HP:0000121

Decreased circulating T4 concentration

Occasional (5-29%)HP:0031507

High blood phosphate levels

Occasional (5-29%)HP:0002905

Hypoglycemic episodes

Occasional (5-29%)HP:0001988

Increased proinsulin:insulin ratio

Occasional (5-29%)HP:0031883

Metabolic acidosis

Occasional (5-29%)HP:0001942

Subclinical abnormal liver function tests

Occasional (5-29%)HP:0002910

Thyroid-stimulating hormone excess

Occasional (5-29%)HP:0002925

Abnormality of the abdomen

HP:0001438

Abnormality of tryptophan metabolism

HP:0004365

Related Conditions

Disorder of tryptophan metabolism(parent)

Microscopic nephrocalcinosis(parent)

Malabsorption syndrome(parent)

Quick Facts

SNOMED CT: 59531002
UMLS CUI: C0268478
Fully Specified Name: Tryptophan malabsorption syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 14

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.