Megaloblastic anemia due to impaired absorption of folate

disorder

SNOMED 27798002CUI C0271943

Overview

Megaloblastic anemia due to impaired absorption of folate 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.

Folate-responsive megaloblastic anemia

Always present (100%)HP:0004851

Reduced blood folate concentration

Always present (100%)HP:0100507

Susceptibility to infection

Always present (100%)HP:0002719

Abnormality of movement

Very frequent (80-99%)HP:0100022

Decreased circulating immunoglobulin concentration

Very frequent (80-99%)HP:0004313

Diarrhea

Very frequent (80-99%)HP:0002014

Immunological abnormality

Very frequent (80-99%)HP:0002715

Inflammation of the tongue

Very frequent (80-99%)HP:0000206

Megaloblastic anemia

Very frequent (80-99%)HP:0001889

Nausea and vomiting

Very frequent (80-99%)HP:0002017

Obsessive dieting

Very frequent (80-99%)HP:0002039

Paleness

Very frequent (80-99%)HP:0000980

Poor weight gain

Very frequent (80-99%)HP:0001508

Psychomotor development deficiency

Very frequent (80-99%)HP:0001263

Red and sore lips

Very frequent (80-99%)HP:0100825

Behavioral changes

Frequent (30-79%)HP:0000708

Epilepsy

Frequent (30-79%)HP:0001250

Gastro-esophageal reflux

Frequent (30-79%)HP:0002020

Neuropathy

Frequent (30-79%)HP:0009830

Abnormal deposits of calcium in the brain

Occasional (5-29%)HP:0002514

Eosinophilia

Occasional (5-29%)HP:0001880

Immune deficiency

Occasional (5-29%)HP:0002721

Increased reflexes

Occasional (5-29%)HP:0001347

Low platelet count

Occasional (5-29%)HP:0001873

Muscle degeneration

Occasional (5-29%)HP:0003202

Pancytopenia

Occasional (5-29%)HP:0001876

Repeated bladder infections

Occasional (5-29%)HP:0000010

respiratory infections, recurrent

Occasional (5-29%)HP:0002205

Ataxia

HP:0001251

Athetoid movements

HP:0002305

Related Conditions

Megaloblastic anemia due to disease of small intestine(child)

Megaloblastic anemia due to pregnancy(child)

Megaloblastic anemia due to folate deficiency(parent)

Quick Facts

SNOMED CT: 27798002
UMLS CUI: C0271943
Fully Specified Name: Megaloblastic anemia due to impaired absorption of folate (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.