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Aplasia cutis congenita with intestinal lymphangiectasia syndrome

disorder
SNOMED 720500008CUI C4304031

Overview

Aplasia cutis congenita with intestinal lymphangiectasia 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.

Abnormal hair quantity
Very frequent (80-99%)HP:0011362
Bilateral single transverse palmar creases
Very frequent (80-99%)HP:0007598
Calvarial defect
Very frequent (80-99%)HP:0001362
Onset of lymphedema around puberty
Very frequent (80-99%)HP:0001004
Absolute lymphocyte count decrease
Frequent (30-79%)HP:0001888
Curvature of little finger
Frequent (30-79%)HP:0004209
Decreased circulating immunoglobulin concentration
Frequent (30-79%)HP:0004313
Hypoproteinemia
Frequent (30-79%)HP:0003075
Intestinal malabsorption
Frequent (30-79%)HP:0002024
Bleeding tendency
Occasional (5-29%)HP:0001892
Blood coagulation disorder
Occasional (5-29%)HP:0001928
Coloboma of choroid
Occasional (5-29%)HP:0000567
Near sighted
Occasional (5-29%)HP:0000545

Quick Facts

SNOMED CT
720500008
UMLS CUI
C4304031
Fully Specified Name
Aplasia cutis congenita with intestinal lymphangiectasia syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
13
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.

Aplasia cutis congenita with intestinal lymphangiectasia syndrome — Symptoms, Testing & Specialists | Healos | Healos