400962005: Congenital miosis (disorder)

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

\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Finding of head region\Globe finding (finding)\Pupil finding\Finding of appearance of pupil\Finding of size of pupil (finding)\Constricted pupil\Congenital miosis (disorder)
\Head finding (finding)\Finding of head region\Globe finding (finding)\Pupil finding\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Head finding (finding)\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)

\Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Eye / vision finding\Globe finding (finding)\Pupil finding\Finding of appearance of pupil\Finding of size of pupil (finding)\Constricted pupil\Congenital miosis (disorder)
\Eye / vision finding\Globe finding (finding)\Pupil finding\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Eye / vision finding\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)

\Functional finding\Constricted pupil\Congenital miosis (disorder)

\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Pupillary disorder (disorder)\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Disorder of head (disorder)\Congenital anomaly of head\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)
\Disease\Developmental disorder (disorder)\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Congenital anomaly of pupil\Congenital miosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital miosis (disorder)	Is a	Miosis	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital miosis (disorder)	Is a	Congenital anomaly of iris	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital miosis (disorder)	Finding site	Iris structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Finding site	Pupil structure (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital miosis (disorder)	Finding site	Iridial and/or ciliary structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital miosis (disorder)	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital miosis (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital miosis (disorder)	Finding site	Iris structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Associated morphology	anomalie congénitale	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Associated morphology	anomalie du développement	false	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital miosis (disorder)	Finding site	Iris structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Is a	Constricted pupil	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital miosis (disorder)	Interprets	Pupil constriction (observable entity)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Congenital miosis (disorder)	Is a	Congenital anomaly of pupil	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital miosis (disorder)	Finding site	Pupil structure (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Congenital miosis (disorder)	Interprets	Size of pupil	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Congenital miosis (disorder)	Associated morphology	Abnormal smallness (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Thrombocytopathy, asplenia and miosis (disorder)	Is a	True	Congenital miosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)
Spastic ataxia with congenital miosis is a rare hereditary ataxia characterized by an apparently non-progressive or slowly progressive symmetrical ataxia of gait, pyramidal signs in the limbs, spasticity and hyperreflexia (especially in the lower limbs) together with dysarthria and impaired pupillary reaction to light, presenting as a fixed miosis (with pupils that seldom exceed 2 mm in diameter and dilate poorly with mydriatics). Nystagmus may also be present.	Is a	True	Congenital miosis (disorder)	Inferred relationship	Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
1768883010	Congenital miosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1780170017	Congenital miosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1768883010	Congenital miosis (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1768883010	Congenital miosis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1780170017	Congenital miosis	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
1780170017	Congenital miosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
526641000274117	Kongenitale Mikrokorie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
609951000274118	Kongenitale Miosis	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5874001000241116	myosis congénital	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
5874001000241116	myosis congénital	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
526641000274117	Kongenitale Mikrokorie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
609951000274118	Kongenitale Miosis	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3397011001000117	Mikrokorie, kongenitale	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module