438504004: Lenz microphthalmia syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Finding of head and neck region\Head finding\...

\Finding of head region\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Finding of head region\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome

\Disorder of head\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome

\Eye / vision finding\Globe finding\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system\Lenz microphthalmia syndrome
\Eye / vision finding\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the visual system\Lenz microphthalmia syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Lenz microphthalmia syndrome
\Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked recessive hereditary disease\Lenz microphthalmia syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the visual system\Lenz microphthalmia syndrome
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system\Lenz microphthalmia syndrome
\Disease\Disorder of body system\Visual system disorder\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Disorder of head\Disorder of eye region\Disorder of eye proper\Anomaly of eye\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Disorder of head\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Lenz microphthalmia syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of visual system\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of head\Congenital anomaly of eye\Microphthalmos\Lenz microphthalmia syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2009. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

2788681016 Lenz microphthalmia syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

2791289019 Lenz microphthalmia syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Lenz microphthalmia syndrome	Is a	X-linked hereditary disease	false	Inferred relationship	Existential restriction modifier
Lenz microphthalmia syndrome	Is a	Hereditary disorder of the visual system	true	Inferred relationship	Existential restriction modifier
Lenz microphthalmia syndrome	Is a	Microphthalmos	true	Inferred relationship	Existential restriction modifier
Lenz microphthalmia syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Lenz microphthalmia syndrome	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier	2
Lenz microphthalmia syndrome	Finding site	Entire eye	false	Inferred relationship	Existential restriction modifier	2
Lenz microphthalmia syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Associated morphology	Congenital smallness	true	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Finding site	Entire eye	true	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Lenz microphthalmia syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier
Lenz microphthalmia syndrome	Is a	X-linked recessive hereditary disease	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2788681016	Lenz microphthalmia syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2791289019	Lenz microphthalmia syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module