Familial pulmonary capillary haemangiomatosis

disorder

SNOMED 234161007CUI C0340848

Overview

Familial pulmonary capillary haemangiomatosis 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.

Difficulty breathing

Always present (100%)HP:0002094

Centrilobular ground-glass opacification on pulmonary HRCT

Very frequent (80-99%)HP:0025180

Decreased DLCO

Very frequent (80-99%)HP:0045051

Chronic extreme exhaustion

Frequent (30-79%)HP:0012432

Swollen lymph nodes in centre of chest

Frequent (30-79%)HP:0100721

Coughing

HP:0012735

Pulmonary artery hypertension

HP:0002092

Pulmonary hemangiomas

HP:0005954

Pulmonary venoocclusive disease

HP:0006518

Related Conditions

Pulmonary capillary haemangiomatosis(parent)

Familial disease(parent)

Recessive hereditary disorder (autosomal)(parent)

Cardiovascular system hereditary disorder(parent)

Quick Facts

SNOMED CT: 234161007
UMLS CUI: C0340848
Fully Specified Name: Familial pulmonary capillary hemangiomatosis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 9

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.