82837002: Kenny syndrome (disorder)

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

\Finding of neck region\Disease of neck\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Idiopathic hypoparathyroidism\Kenny syndrome

\Functional finding\Decline in functional status (finding)\Decreased hormone secretion\Hypoparathyroidism\Idiopathic hypoparathyroidism\Kenny syndrome

\Endocrine finding\Decreased hormone secretion\Hypoparathyroidism\Idiopathic hypoparathyroidism\Kenny syndrome

\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Osteochondrodysplasia syndrome\Kenny syndrome
\Disease\Disorder of body system\Disorder of endocrine system (disorder)\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Idiopathic hypoparathyroidism\Kenny syndrome
\Disease\Disease of neck\Disorder of parathyroid gland (disorder)\Hypoparathyroidism\Idiopathic hypoparathyroidism\Kenny syndrome
\Disease\Idiopathic disease\Idiopathic hypoparathyroidism\Kenny syndrome
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Osteochondrodysplasia syndrome\Kenny syndrome

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
Kenny syndrome	Is a	Osteochondrodysplasia syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Is a	Idiopathic hypoparathyroidism	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Is a	Congenital anomaly of parathyroid glands (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Finding site	Parathyroid structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Kenny syndrome	Interprets	Nutritional deficiency state	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Is a	Congenital anomaly of neck	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Is a	Congenital anomaly of endocrine gland	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Has definitional manifestation	Decreased hormone secretion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Kenny syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Kenny syndrome	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Kenny syndrome	Interprets	Hormone secretion	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Kenny syndrome	Has interpretation	Decreased	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Kenny syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Kenny syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Syndromic nanophthalmos due to Kenny-Caffey syndrome (disorder)	Due to	True	Kenny syndrome	Inferred relationship	Existential restriction modifier (core metadata concept)	2

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
137411019	Kenny syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
505290013	Kenny-Caffey syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
824343010	Kenny syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
137411019	Kenny syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
505290013	Kenny-Caffey syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
824343010	Kenny syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
824343010	Kenny syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3422131001000113	Kenny-Caffey-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4660431000241118	syndrome de Kenny-Caffey	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4660431000241118	syndrome de Kenny-Caffey	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3422131001000113	Kenny-Caffey-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module