Hereditary macular atrophy

disorder

SNOMED 733467001CUI C4518793

Overview

Hereditary macular atrophy 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.

Papules

Very frequent (80-99%)HP:0200034

Abnormal tibia morphology

Frequent (30-79%)HP:0002992

Generalized joint laxity

Frequent (30-79%)HP:0002761

Increased lumbar lordosis

Frequent (30-79%)HP:0002938

Irregular teeth

Frequent (30-79%)HP:0040079

Narrow, high-arched roof of mouth

Frequent (30-79%)HP:0002705

Related Conditions

Autosomal hereditary disorder(parent)

Atrophoderma maculatum(parent)

Hereditary disorder of the integument(parent)

Congenital anomaly of skin(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 733467001
UMLS CUI: C4518793
Fully Specified Name: Hereditary anetoderma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.