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Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome

disorder
SNOMED 723829000CUI C4510085

Overview

Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia 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.

Hepatosplenomegaly
Very frequent (80-99%)HP:0001433
Hypoplastic bone marrow
Very frequent (80-99%)HP:0005528
Partial nodular transformation of liver
Very frequent (80-99%)HP:0011954
Portal hypertension
Very frequent (80-99%)HP:0001409
Pulmonary fibrosis
Very frequent (80-99%)HP:0002206
Abnormal liver function tests
Frequent (30-79%)HP:0002910
Abnormality of liver blood vessels
Frequent (30-79%)HP:0006707
Coughing
Frequent (30-79%)HP:0012735
Difficulty breathing
Frequent (30-79%)HP:0002094
Increased ferritin
Frequent (30-79%)HP:0003281
Low platelet count
Frequent (30-79%)HP:0001873
Rales
Frequent (30-79%)HP:0030830
Restrictive respiratory disease
Frequent (30-79%)HP:0002091
Abnormal lung auscultation finding
Occasional (5-29%)HP:0030829
Abnormal pleura morphology
Occasional (5-29%)HP:0002103
Myocardial fibrosis
Occasional (5-29%)HP:0001685

Quick Facts

SNOMED CT
723829000
UMLS CUI
C4510085
Fully Specified Name
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
16
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.