Hereditary acrodermatitis enteropathica

disorder

SNOMED 37702000CUI C0221036

Overview

Hereditary acrodermatitis enteropathica 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.

Perianal erythema

Always present (100%)HP:0033195

Perioral erythema

Always present (100%)HP:0033194

Abnormal blistering of the skin

Very frequent (80-99%)HP:0008066

Abnormality of the eyebrow

Very frequent (80-99%)HP:0000534

Abnormality of the eyelids

Very frequent (80-99%)HP:0000492

Cerebral cortex atrophy

Very frequent (80-99%)HP:0002120

Chronic diarrhoea

Very frequent (80-99%)HP:0002028

Decreased body height

Very frequent (80-99%)HP:0004322

Erythema

Very frequent (80-99%)HP:0010783

Generalized abnormality of skin

Very frequent (80-99%)HP:0011354

Hair loss

Very frequent (80-99%)HP:0001596

Intestinal malabsorption

Very frequent (80-99%)HP:0002024

Pimple

Very frequent (80-99%)HP:0200039

Xerosis

Very frequent (80-99%)HP:0000958

Abnormal nail morphology

Frequent (30-79%)HP:0001597

Blepharitis

Frequent (30-79%)HP:0000498

Conjunctivitis

Frequent (30-79%)HP:0000509

Decreased serum zinc

Frequent (30-79%)HP:0031831

Diarrhea

Frequent (30-79%)HP:0002014

Emotional lability

Frequent (30-79%)HP:0000712

Glossal abnormality

Frequent (30-79%)HP:0000157

Inflammation of the tongue

Frequent (30-79%)HP:0000206

Lingua plicata

Frequent (30-79%)HP:0000221

Longitudinal ridging

Frequent (30-79%)HP:0001807

Open skin sore

Frequent (30-79%)HP:0200042

Paronychia

Frequent (30-79%)HP:0001818

Photophobia

Frequent (30-79%)HP:0000613

Red and sore lips

Frequent (30-79%)HP:0100825

Ridged fingernails

Frequent (30-79%)HP:0008402

Undergrowth

Frequent (30-79%)HP:0001508

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Disorder of zinc metabolism(parent)

Hereditary disorder of the integument(parent)

Gianotti-Crosti syndrome(parent)

Quick Facts

SNOMED CT: 37702000
UMLS CUI: C0221036
Fully Specified Name: Hereditary acrodermatitis enteropathica (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.