254150007: Francois syndrome (disorder)

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

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Nodule in skin or mucosa\Skin nodule\Francois syndrome
\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane (disorder)\Skin lesion\Skin nodule\Francois syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Mass of skin\Skin nodule\Francois syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Francois syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Skin nodule\Francois syndrome

\Mass of body structure\Mass of soft tissue\Mass of skin\Skin nodule\Francois syndrome
\Mass of body structure\Mass of body region (finding)\Mass of skin\Skin nodule\Francois syndrome
\Mass of body structure\Nodule in skin or mucosa\Skin nodule\Francois syndrome

\General finding of soft tissue\Mass of soft tissue\Mass of skin\Skin nodule\Francois syndrome
\General finding of soft tissue\Skin finding\Mass of skin\Skin nodule\Francois syndrome
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Francois syndrome
\General finding of soft tissue\Skin finding\Disorder of skin (disorder)\Skin lesion\Skin nodule\Francois syndrome
\General finding of soft tissue\Disorder of soft tissue\Lesion of soft tissue (disorder)\Skin lesion\Skin nodule\Francois syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Francois syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Skin nodule\Francois syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument (disorder)\Francois syndrome
\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Congenital anomaly of integument\Congenital anomaly of skin (disorder)\Francois syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Francois syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue (disorder)\Disorder of skin (disorder)\Skin lesion\Skin nodule\Francois syndrome
\Integumentary system finding\Skin finding\Mass of skin\Skin nodule\Francois syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Congenital anomaly of skin (disorder)\Francois syndrome
\Integumentary system finding\Skin finding\Disorder of skin (disorder)\Skin lesion\Skin nodule\Francois syndrome

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

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Francois syndrome	Is a	Disease of eye	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Disorder of integument	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Multisystem disorder E-F	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Disorder of musculoskeletal system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Finding site	Structure of skin region (body structure)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Finding site	Eye structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	trouble multisytémique	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Visual system disorder	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Disorder of bone (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Disorder of skin (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Finding site	The eye, ocular adnexa, afferent visual pathways, efferent visual pathways, and pupil innervation pathways	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Site-specific disorder of skin	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Morquio syndrome (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Hereditary corneal dystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Associated morphology	Dystrophy	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Francois syndrome	Finding site	Bone structure	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Francois syndrome	Finding site	Corneal structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Francois syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Francois syndrome	Is a	Congenital structural abnormality of cornea	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Congenital anomaly of skin (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Congenital anomaly of skeletal bone	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Congenital osteodystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Skin lesion	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Finding site	Bone structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Francois syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Francois syndrome	Is a	Hereditary disorder of musculoskeletal system	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Hereditary disorder of the integument (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Francois syndrome	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Associated morphology	Dystrophy	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Francois syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Is a	Skin nodule	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Associated morphology	Nodule	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Francois syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Francois syndrome	Is a	Congenital dystrophy of cornea (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
378327015	Dermochondrocorneal dystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
378328013	Francois syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
645001013	Francois syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
378327015	Dermochondrocorneal dystrophy	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
378327015	Dermochondrocorneal dystrophy	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
378328013	Francois syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
645001013	Francois syndrome (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
645001013	Francois syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
529871000274117	Dermo-chondro-corneale Dystrophie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
621451000274119	Francois-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
146631000077116	syndrome de François	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
146631000077116	syndrome de François	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
529871000274117	Dermo-chondro-corneale Dystrophie	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
621451000274119	Francois-Syndrom	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3437871001000118	Dystrophie, dermo-chondro-corneale	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module