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66091009: Congenital disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
109766011 Congenital disease en Synonym Active Entire term case insensitive SNOMED CT core module
500308011 Congenital disorder en Synonym Active Entire term case insensitive SNOMED CT core module
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

9730 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital disease Is a Disease true Inferred relationship Existential restriction modifier
Congenital disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked corneal dermoid Is a True Congenital disease Inferred relationship Existential restriction modifier
X-linked neurodegenerative syndrome Bertini type Is a True Congenital disease Inferred relationship Existential restriction modifier
Isolated generalized anhidrosis with normal sweat glands Is a True Congenital disease Inferred relationship Existential restriction modifier
Non-syndromic mitochondrial sensorineural deafness Is a True Congenital disease Inferred relationship Existential restriction modifier
Nemaline myopathy, early onset type Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital palsy of trochlear nerve Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital oculomotor nerve palsy Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital horizontal gaze palsy Is a True Congenital disease Inferred relationship Existential restriction modifier
Isolated congenital horizontal gaze paresis Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital monocular elevator palsy Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital isolated adrenocorticotropic hormone deficiency Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital pseudopapilledema Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital insensitivity to pain with severe intellectual disability Is a True Congenital disease Inferred relationship Existential restriction modifier
Congenital axonal neuropathy with encephalopathy Is a True Congenital disease Inferred relationship Existential restriction modifier
Simpson-Golabi-Behmel syndrome Is a False Congenital disease Inferred relationship Existential restriction modifier
[X]Additional congenital disease classification terms Is a False Congenital disease Inferred relationship Existential restriction modifier
[X]Other specified congenital malformations of integument Is a False Congenital disease Inferred relationship Existential restriction modifier
Integument anomalies NOS Is a False Congenital disease Inferred relationship Existential restriction modifier
Other congenital anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier
Other specified integument anomaly Is a False Congenital disease Inferred relationship Existential restriction modifier
Other and unspecified congenital anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier
Other specified face and neck anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier
Other specified nonteratogenic anomalies Is a False Congenital disease Inferred relationship Existential restriction modifier
Unspecified anomaly of connective tissue Is a False Congenital disease Inferred relationship Existential restriction modifier
Central nervous system (SNC)/head/neck congenital anomaly NOS Is a False Congenital disease Inferred relationship Existential restriction modifier
History of - congenital anomaly NOS Associated finding False Congenital disease Inferred relationship Existential restriction modifier 1
Family history: Congenital anomaly NOS Associated finding False Congenital disease Inferred relationship Existential restriction modifier 1
Suspected congenital abnormality Associated finding True Congenital disease Inferred relationship Existential restriction modifier 1

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