FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.10 | FHIR Version n/a User: [n/a]

38196001: Laron-type isolated somatotropin defect (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Body measurement finding\Height / growth finding\General finding of height\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect

\Finding of general physiological development\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect

\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Laron-type isolated somatotropin defect
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Laron-type isolated somatotropin defect
\Disease\Developmental disorder\Developmental hereditary disorder\Laron-type isolated somatotropin defect
\Disease\Developmental disorder\Disorder of stature\Short stature disorder\Laron-type isolated somatotropin defect

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Laron-type isolated somatotropin defect	Is a	Pituitary dwarfism	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Is a	Short stature disorder	true	Inferred relationship	Some
Laron-type isolated somatotropin defect	Associated morphology	Developmental anomaly	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Interprets	Nutritional deficiency (finding)	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Finding site	Pars anterior of pituitary gland	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Associated morphology	Congenital deficiency	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Finding site	Adenohypophysis structure	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Occurrence	Congenital	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Some
Laron-type isolated somatotropin defect	Is a	Dwarfism	false	Inferred relationship	Some
Laron-type isolated somatotropin defect	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Laron-type isolated somatotropin defect	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Laron-type isolated somatotropin defect	Interprets	Height / growth measure	true	Inferred relationship	Some	2

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Growth hormone receptor absent	Is a	True	Laron-type isolated somatotropin defect	Inferred relationship	Some
Growth hormone receptor abnormality	Is a	True	Laron-type isolated somatotropin defect	Inferred relationship	Some

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
63917019	Laron-type isolated somatotropin defect	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
63918012	Laron-type dwarfism	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
63919016	Laron dwarfism	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
63920010	Laron-type pituitary dwarfism	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
771912011	Laron-type isolated somatotropin defect (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4535149016	Laron syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core