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Hereditary factor I deficiency disease

disorder
SNOMED 31925001CUI C0019250

Overview

Hereditary factor I deficiency disease 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.

Afibrinogenemia
Always present (100%)HP:0034287
Abnormal umbilical stump bleeding
Very frequent (80-99%)HP:0011884
Abnormality of cardiovascular system morphology
Very frequent (80-99%)HP:0030680
Abnormality of the subungual region
Very frequent (80-99%)HP:0009723
Anaphylaxis
Very frequent (80-99%)HP:0100845
Arc de cercle
Very frequent (80-99%)HP:0002179
Bleeding below the skin
Very frequent (80-99%)HP:0001933
Bleeding gums
Very frequent (80-99%)HP:0000225
Bleeding tendency
Very frequent (80-99%)HP:0001892
Blue discoloration of the skin
Very frequent (80-99%)HP:0000961
Bruising susceptibility
Very frequent (80-99%)HP:0000978
Cataract, congenital
Very frequent (80-99%)HP:0000519
Clubbing of fingers
Very frequent (80-99%)HP:0100759
Decreased testicular size
Very frequent (80-99%)HP:0008734
Elevated heart rate
Very frequent (80-99%)HP:0001649
Frequent nosebleeds
Very frequent (80-99%)HP:0000421
Hemorrhagic ovarian cyst
Very frequent (80-99%)HP:0012886
Internal bleeding
Very frequent (80-99%)HP:0011029
Joint swelling
Very frequent (80-99%)HP:0001386
Left ventricular wall hypertrophy
Very frequent (80-99%)HP:0001712
Loss of consciousness
Very frequent (80-99%)HP:0007185
Low factor II activity
Very frequent (80-99%)HP:0008151
Menometrorrhagia
Very frequent (80-99%)HP:0400008
Nanophthalmos
Very frequent (80-99%)HP:0000568
Pyrexia
Very frequent (80-99%)HP:0001945
Right ventricular hypertrophy
Very frequent (80-99%)HP:0001667
Ruptured spleen
Very frequent (80-99%)HP:0012223
Short penis
Very frequent (80-99%)HP:0000054
Upset stomach
Very frequent (80-99%)HP:0002027
Volvulus
Very frequent (80-99%)HP:0002580

Related Conditions

Congenital hypofibrinogenemia(child)
Congenital dysfibrinogenemia(child)
Congenital afibrinogenemia(child)
Hypodysfibrinogenaemia(child)
Congenital fibrinogen abnormality(parent)
Hereditary coagulation factor deficiency(parent)
Autosomal hereditary disorder(parent)
Factor I deficiency disease(parent)

Quick Facts

SNOMED CT
31925001
UMLS CUI
C0019250
Fully Specified Name
Hereditary factor I deficiency disease (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
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.