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Primary haemochromatosis

disorder
SNOMED 399170009CUI C0392514

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal glucose tolerance
HP:0001952
Abnormal heart rate
HP:0011675
Amenorrhea
HP:0000141
Ascites
HP:0001541
Azoospermia
HP:0000027
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
Hair loss
HP:0001596
Heart failure
HP:0001635
Increased circulating iron concentration
HP:0003452
Increased heart size
HP:0001640
Increased incidence of hepatocellular carcinoma
HP:0001402
Increased serum ferritin level
HP:0003281
Isolated hypogonadotropic hypogonadism
HP:0000044
Large spleen
HP:0001744
Melanoderma
HP:0000953
Osteoporosis
HP:0000939
Telangiectasia
HP:0001009
Testicular degeneration
HP:0000029
Upset stomach
HP:0002027

Related Conditions

Quick Facts

SNOMED CT
399170009
UMLS CUI
C0392514
Fully Specified Name
Primary hemochromatosis (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.