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Hereditary infantile gigantism

disorder
SNOMED 773645004CUI C4751112

Overview

Hereditary infantile gigantism 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.

Abnormal pituitary gland morphology
Very frequent (80-99%)HP:0012503
Accelerated linear growth
Very frequent (80-99%)HP:0000098
Elevated circulating growth hormone concentration
Very frequent (80-99%)HP:0000845
Increased circulating insulin-like growth factor 1 concentration
Very frequent (80-99%)HP:0030269
Prolactin excess
Very frequent (80-99%)HP:0000870
Abnormal oral glucose tolerance
Frequent (30-79%)HP:0004924
Abnormality of optic chiasm morphology
Frequent (30-79%)HP:0025163
Coarse face
Frequent (30-79%)HP:0000280
Decreased thyrotropin level
Frequent (30-79%)HP:0031098
Fasting hyperinsulinemia
Frequent (30-79%)HP:0008283
Hyperhidrosis
Frequent (30-79%)HP:0000975
Hyperphagia
Frequent (30-79%)HP:0002591
Increased BMI
Frequent (30-79%)HP:0031418
Pachydermia
Frequent (30-79%)HP:0001072
Pituitary adenoma
Frequent (30-79%)HP:0002893
Sleep apnea
Frequent (30-79%)HP:0010535
Snoring symptoms
Frequent (30-79%)HP:0025267
Acanthosis nigricans
Occasional (5-29%)HP:0000956
ACTH deficiency
Occasional (5-29%)HP:0011748
Ataxia
Occasional (5-29%)HP:0001251
Belly bloating
Occasional (5-29%)HP:0003270
Cardiovascular disease
Occasional (5-29%)HP:0001626
Decreased activity of gonads
Occasional (5-29%)HP:0000135
Delayed puberty
Occasional (5-29%)HP:0000823
Diabetes insipidus
Occasional (5-29%)HP:0000873
Disproportionately large hands
Occasional (5-29%)HP:0001176
Enlarged pituitary gland
Occasional (5-29%)HP:0012505
Gaps between teeth
Occasional (5-29%)HP:0000699
Headache
Occasional (5-29%)HP:0002315
Hypopituitarism
Occasional (5-29%)HP:0040075

Related Conditions

X-linked acrogigantism due to Xq26 microduplication(child)
Hypersomatotropic gigantism(parent)
Hereditary disorder of nervous system(parent)
Hereditary disorder of endocrine system(parent)
Developmental hereditary disorder(parent)
X-linked dominant hereditary disease(parent)

Quick Facts

SNOMED CT
773645004
UMLS CUI
C4751112
Fully Specified Name
Familial infantile gigantism (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.