Growth delay due to insulin-like growth factor type 1 deficiency

disorder

SNOMED 724385009CUI C1837475

Overview

Growth delay due to insulin-like growth factor type 1 deficiency 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.

Decreased body weight

Always present (100%)HP:0004325

Decreased serum insulin-like growth factor 1

Always present (100%)HP:0030353

Elevated circulating growth hormone concentration

Always present (100%)HP:0000845

Osteopenia

Always present (100%)HP:0000938

Behavioral symptoms

Very frequent (80-99%)HP:0000708

Bilateral nerve deafness

Very frequent (80-99%)HP:0008619

Body fails to respond to insulin

Very frequent (80-99%)HP:0000855

Childhood attention deficit/hyperactivity disorder

Very frequent (80-99%)HP:0007018

Congenital neurosensory deafness

Very frequent (80-99%)HP:0008527

Decreased body height

Very frequent (80-99%)HP:0004322

Decreased size of cranium

Very frequent (80-99%)HP:0000252

Deformity of face

Very frequent (80-99%)HP:0001999

Dull intelligence

Very frequent (80-99%)HP:0001249

Growth delay as children

Very frequent (80-99%)HP:0008897

hyperkinetic disorder

Very frequent (80-99%)HP:0000752

Intrauterine growth retardation, IUGR

Very frequent (80-99%)HP:0001511

Low birth weight

Very frequent (80-99%)HP:0001518

Marked growth retardation

Very frequent (80-99%)HP:0008850

Mental retardation, mild

Very frequent (80-99%)HP:0001256

Poor attention span

Very frequent (80-99%)HP:0000736

Postnatal failure to thrive

Very frequent (80-99%)HP:0001508

Prelingual sensorineural hearing impairment

Very frequent (80-99%)HP:0000399

Sensorineural deafness

Very frequent (80-99%)HP:0000407

Severe intrauterine growth retardation

Very frequent (80-99%)HP:0008846

Abnormal mouth

Frequent (30-79%)HP:0000153

Curvature of digit

Frequent (30-79%)HP:0030084

Curvature of little finger

Frequent (30-79%)HP:0004209

Decreased activity of gonads

Frequent (30-79%)HP:0000135

Delayed eruption of teeth

Frequent (30-79%)HP:0000684

Hyperbilirubinemia, neonatal

Frequent (30-79%)HP:0003265

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Congenital disease(parent)

Hereditary growth hormone deficiency(parent)

Quick Facts

SNOMED CT: 724385009
UMLS CUI: C1837475
Fully Specified Name: Growth delay due to insulin-like growth factor type 1 deficiency (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.