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82837002: Kenny syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
137411019 Kenny syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
505290013 Kenny-Caffey syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
824343010 Kenny syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Kenny syndrome Is a Osteochondrodysplasia syndrome true Inferred relationship Existential restriction modifier
Kenny syndrome Is a Idiopathic hypoparathyroidism true Inferred relationship Existential restriction modifier
Kenny syndrome Is a Congenital anomaly of parathyroid glands false Inferred relationship Existential restriction modifier
Kenny syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Kenny syndrome Finding site Entire endocrine gonad false Inferred relationship Existential restriction modifier
Kenny syndrome Finding site Parathyroid structure true Inferred relationship Existential restriction modifier 3
Kenny syndrome Interprets Nutritional deficiency false Inferred relationship Existential restriction modifier
Kenny syndrome Is a Congenital anomaly of neck false Inferred relationship Existential restriction modifier
Kenny syndrome Is a Congenital anomaly of endocrine gland false Inferred relationship Existential restriction modifier
Kenny syndrome Has definitional manifestation Decreased hormone secretion false Inferred relationship Existential restriction modifier
Kenny syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Kenny syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Kenny syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Kenny syndrome Interprets Hormone secretion, function true Inferred relationship Existential restriction modifier 2
Kenny syndrome Has interpretation Decreased true Inferred relationship Existential restriction modifier 2
Kenny syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Kenny syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

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

This concept is not in any reference sets

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