715625007: Growth delay due to insulin-like growth factor I resistance (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Finding of general physiological development\Disorder of stature\Short stature disorder\Growth delay due to insulin-like growth factor I resistance
• \General finding of observation of patient\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Growth delay due to insulin-like growth factor I resistance
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Growth delay due to insulin-like growth factor I resistance
• \Disease\Developmental disorder\Developmental hereditary disorder\Growth delay due to insulin-like growth factor I resistance
• \Disease\Developmental disorder\Disorder of stature\Short stature disorder\Growth delay due to insulin-like growth factor I resistance

Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3303207018	Growth delay due to insulin-like growth factor I resistance (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3303208011	Growth delay due to insulin-like growth factor I resistance	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3303209015	Growth delay due to insulin-like growth factor 1 resistance	en	Synonym	Active	Case insensitive	SNOMED CT core
3303210013	IGF-1 (insulin-like growth factor 1) resistance	en	Synonym	Active	Case sensitive	SNOMED CT core
3303211012	Somatomedin C resistance	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3302601019	Variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Additional features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum). Prevalence is unknown, may be caused by a variety of genetic defects.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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