715625007: groeiachterstand door resistentie tegen insulineachtige groeifactor 1 (aandoening)

• SNOMED CT Concept\Clinical finding (finding)\...
• \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 (disorder)
• \Finding of general physiological development\Disorder of stature\Short stature disorder\Growth delay due to insulin-like growth factor I resistance (disorder)
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Growth delay due to insulin-like growth factor I resistance (disorder)
• \Disease\Developmental disorder\Developmental hereditary disorder\Growth delay due to insulin-like growth factor I resistance (disorder)
• \Disease\Developmental disorder\Disorder of stature\Short stature disorder\Growth delay due to insulin-like growth factor I resistance (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303208011	Growth delay due to insulin-like growth factor I resistance	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3303209015	Growth delay due to insulin-like growth factor 1 resistance	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3303210013	IGF-1 (insulin-like growth factor 1) resistance	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3303211012	Somatomedin C resistance	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6476661000146112	groeiachterstand door resistentie tegen insulineachtige groeifactor I	nl	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6476671000146118	groeiachterstand door resistentie tegen insulineachtige groeifactor I (aandoening)	nl	Fully specified name	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6476701000146119	groeivertraging door resistentie tegen somatomedine C	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6701271000146111	groeivertraging door resistentie tegen 'insulin-like growth factor I'	nl	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
6701281000146113	groeivertraging door IGF-I-resistentie	nl	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12576461000146116	groeiachterstand door resistentie tegen insulineachtige groeifactor 1 (aandoening)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12576471000146110	groeiachterstand door resistentie tegen insulineachtige groeifactor 1	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12576481000146112	groeivertraging door IGF-1-resistentie	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
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	Entire term case sensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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