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Haemochromatosis type 1

disorder
SNOMED 1186847009CUI C3469186

Overview

Haemochromatosis type 1 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.

Amenorrhea
HP:0000141
Azoospermia
HP:0000027
Cardiac arrhythmias
HP:0011675
Chronic heart failure
HP:0001635
Cirrhosis
HP:0001394
Diabetes mellitus
HP:0000819
Difficulty getting an erection
HP:0000802
Disease of the heart muscle
HP:0001638
Disease of the joints
HP:0003040
Elevated serum transaminases
HP:0002910
Enlarged liver
HP:0002240
Fluid around lungs
HP:0002202
Gastro pain
HP:0002027
Glucose intolerance
HP:0001952
Hair loss
HP:0001596
Increased circulating iron concentration
HP:0003452
Increased heart size
HP:0001640
Increased hepatocellular carcinoma risk
HP:0001402
Increased serum ferritin level
HP:0003281
Large spleen
HP:0001744
Low gonadotropins (secondary hypogonadism)
HP:0000044
Melanoderma
HP:0000953
Osteoporosis
HP:0000939
Peritoneal effusion
HP:0001541
Telangiectasia
HP:0001009
Testicular degeneration
HP:0000029

Quick Facts

SNOMED CT
1186847009
UMLS CUI
C3469186
Fully Specified Name
Hemochromatosis type 1 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
26
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.