19010006: Hyaline degeneration (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\Degenerative abnormality\Hyaline degeneration

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

Descriptions:

Id Description Lang Type Status Case? Module

32042011 Hyaline degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

32043018 Hyaline thickening en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

32044012 Hyalinization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

32045013 Hyalinosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

478980011 Hyalinisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

746689017 Hyaline degeneration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hyaline degeneration	Is a	dégénérescence	false	Inferred relationship	Some
Hyaline degeneration	Is a	Degenerative abnormality	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cytoplasmic hyalinization	Is a	True	Hyaline degeneration	Inferred relationship	Some
A rare systemic disease characterized by progressive hyalinosis involving capillaries, arterioles and small veins of the digestive tract, kidneys, and retina, associated with idiopathic cerebral calcifications, manifesting with severe diarrhea (with rectal bleeding and malabsorption), nephropathy (with renal failure and systemic hypertension), chorioretinal scarring, and subarachnoid hemorrhage. Poikiloderma and premature graying of the hair may be additionally observed.	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	4
Salzmann nodular dystrophy	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	2
Salzmann's nodular degeneration of cornea of bilateral eyes (disorder)	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	1
Salzmann's nodular degeneration of cornea of bilateral eyes (disorder)	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	2
Salzmann nodular degeneration of cornea of left eye (disorder)	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	1
Salzmann nodular degeneration of cornea of right eye (disorder)	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	2
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands.	Associated morphology	False	Hyaline degeneration	Inferred relationship	Some	3
A rare genetic disease characterised by infantile or childhood onset of abnormal growth of hyalinised fibrous tissue, giving rise to multiple cutaneous nodules and/or pearly papules predominantly affecting the scalp, ears, neck, face, hands, and feet. Involvement of other organs results in gingival hyperplasia, osteolytic bone lesions, and joint contractures. Some patients exhibit visceral involvement with intractable diarrhoea, increased susceptibility to infections, and severe failure to thrive.	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	3
A rare hyaline fibromatosis syndrome with characteristics of papulo-nodular skin lesions (especially around the head and neck), soft tissue masses, gingival hypertrophy, joint contractures and osteolytic bone lesions in variable degrees. Joint contractures may cripple patients and delay normal motor development if occurring in infancy. Severe gingival hyperplasia can interfere with eating and delay dentition. Histopathology analysis of involved tissues reveals cords of spindle-shaped cells embedded in an amorphous, hyaline material.	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	4
Infantile systemic hyalinosis (ISH) is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterized by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands.	Associated morphology	True	Hyaline degeneration	Inferred relationship	Some	5

Reference Sets