77797009: Hereditary corneal dystrophy (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\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Finding of head region\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Finding of head region\Globe finding (finding)\Anterior segment finding (finding)\Corneal finding\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Finding of head region\Globe finding (finding)\Anterior segment finding (finding)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Finding of head region\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Head finding (finding)\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy

\Eye / vision finding\Globe finding (finding)\Anterior segment finding (finding)\Corneal finding\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Eye / vision finding\Globe finding (finding)\Anterior segment finding (finding)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Eye / vision finding\Globe finding (finding)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Eye / vision finding\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Eye / vision finding\Visual system disorder\Hereditary disorder of the visual system (disorder)\Hereditary corneal dystrophy

\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of sensory organ (disorder)\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system (disorder)\Hereditary disorder of the visual system (disorder)\Hereditary corneal dystrophy
\Disease\Degenerative disorder\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of body system\Hereditary disorder by system (disorder)\Hereditary disorder of the visual system (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of body system\Visual system disorder\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of body system\Visual system disorder\Hereditary disorder of the visual system (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Anomaly of eye\Degenerative disorder of eye (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy
\Disease\Disorder of head (disorder)\Disorder of eye region\Disorder of eye proper (disorder)\Disorder of anterior segment of eye (disorder)\Disease of cornea (disorder)\Corneal degeneration\Corneal dystrophy (disorder)\Hereditary corneal dystrophy

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hereditary corneal dystrophy	Is a	Corneal dystrophy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary corneal dystrophy	Finding site	Corneal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary corneal dystrophy	Is a	Hereditary disorder of the visual system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary corneal dystrophy	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary corneal dystrophy	Finding site	Corneal structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary corneal dystrophy	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Corneal dystrophy unspecified	Is a	False	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Combined corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary corneal dystrophy NOS	Is a	False	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Reis-Bucklers' corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Lattice corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Polymorphous corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital hereditary endothelial dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Fleck corneal dystrophy (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Thiel-Behnke corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Schnyder crystalline cornea dystrophy (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital stromal corneal dystrophy (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Macular corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Ophthalmomandibulomelic dysplasia	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Epithelial recurrent erosion dystrophy of cornea (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Grayson Wilbrandt dystrophy of cornea (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
X-linked endothelial corneal dystrophy (XECD) is a rare subtype of posterior corneal dystrophy characterized by congenital ground glass corneal clouding or a diffuse corneal haze, and blurred vision in male patients.	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Posterior amorphous corneal dystrophy (PACD) is a very rare form of stromal corneal dystrophy characterized by irregular amorphous sheet-like opacities in the posterior corneal stroma and in Descemet membrane and mildly impaired vision.	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Corneal dystrophy-perceptive deafness (CDPD) or Harboyan syndrome is a degenerative corneal disorder characterized by the association of congenital hereditary endothelial dystrophy with progressive, postlingual sensorineural hearing loss.	Is a	False	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Corneal cerebellar syndrome	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Stern Lubinsky Durrie syndrome (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Subepithelial mucinous corneal dystrophy (SMCD) is a very rare form of superficial corneal dystrophy characterized by frequent recurrent corneal erosions in the first decade of life, with progressive loss of vision.	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Lisch epithelial corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
AGel amyloidosis	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Meesman's corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Gelatinous droplike corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Granular corneal dystrophy	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Congenital labioscrotal agenesis, cerebellar malformation, corneal dystrophy, facial dysmorphism syndrome	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Hereditary dystrophy of cornea of bilateral eyes (disorder)	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)
Spondylometaphyseal dysplasia, corneal dystrophy syndrome	Is a	True	Hereditary corneal dystrophy	Inferred relationship	Existential restriction modifier (core metadata concept)

Reference Sets

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Id	Description	Lang	Type	Status	Case?	Module
129114016	Hereditary corneal dystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
818666013	Hereditary corneal dystrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
129114016	Hereditary corneal dystrophy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
129114016	Hereditary corneal dystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
818666013	Hereditary corneal dystrophy (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
818666013	Hereditary corneal dystrophy (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
543031000274111	Erbliche Hornhautdystrophie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
572331000274119	Hereditäre Hornhautdystrophie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4644071000241114	dystrophie de la cornée héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
4644071000241114	dystrophie de la cornée héréditaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
543031000274111	Erbliche Hornhautdystrophie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
572331000274119	Hereditäre Hornhautdystrophie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module