Overview
Kallman syndrome with heart 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.
Low gonadotropins (secondary hypogonadism)
Always present (100%)HP:0000044
Dull intelligence
Very frequent (80-99%)HP:0001249
Total anosmia
Very frequent (80-99%)HP:0010632
Anomalous left coronary artery from the pulmonary artery
Frequent (30-79%)HP:0011638
Blue discoloration of the skin
Frequent (30-79%)HP:0000961
Cardiac murmur
Frequent (30-79%)HP:0030148
Cleft of palate
Frequent (30-79%)HP:0000175
Cryptorchidism, bilateral
Frequent (30-79%)HP:0008689
Decreased body height
Frequent (30-79%)HP:0004322
Decreased testicular size
Frequent (30-79%)HP:0008734
Delayed puberty
Frequent (30-79%)HP:0000823
Double-outlet right ventricle
Frequent (30-79%)HP:0001719
Growth failure
Frequent (30-79%)HP:0001510
Osteopenia
Frequent (30-79%)HP:0000938
Osteoporosis
Frequent (30-79%)HP:0000939
Partial anosmia
Frequent (30-79%)HP:0010633
Renal aplasia
Frequent (30-79%)HP:0000104
Retarded ossification
Frequent (30-79%)HP:0002750
Right aortic arch
Frequent (30-79%)HP:0012020
Sensorineural deafness
Frequent (30-79%)HP:0000407
Short lingual frenum
Frequent (30-79%)HP:0000200
Short penis
Frequent (30-79%)HP:0000054
Stretched and thinned heart muscle
Frequent (30-79%)HP:0001644
Underdeveloped pulmonary artery
Frequent (30-79%)HP:0004971
Aortic valve regurgitation
Occasional (5-29%)HP:0001659
Heart failure
Occasional (5-29%)HP:0001635
Midgut malrotation
Occasional (5-29%)HP:0005211
Mitral regurgitation
Occasional (5-29%)HP:0001653
Puolmonary valve insufficiency
Occasional (5-29%)HP:0010444
Related Conditions
Congenital heart disease(parent)
Recessive hereditary disorder (autosomal)(parent)
Hypogonadism with anosmia(parent)
Cardiovascular system hereditary disorder(parent)
Cardiac complication(parent)
Developmental hereditary disorder(parent)
Hereditary disorder of endocrine system(parent)
Hereditary disorder of nervous system(parent)
Reproductive system hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 722027009
- UMLS CUI
- C4302897
- Fully Specified Name
- Kallman syndrome with heart disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 29
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.