19730000: Abnormally hard consistency (finding)

SNOMED CT Concept\Clinical finding (finding)\Procedure related finding\Evaluation finding\Morphologic finding (finding)\Consistency finding\Abnormally hard consistency

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

33221012 Abnormally hard consistency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

33222017 Hardening en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

748165015 Abnormally hard consistency (finding) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5919821000241119 consistance anormalement dure fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Abnormally hard consistency	Is a	Consistency finding	true	Inferred relationship	Some
Abnormally hard consistency	Finding method (attribute)	Procedure	false	Inferred relationship	Some
Abnormally hard consistency	Interprets	Determination of a value, conclusion, or inference by evaluating evidence	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Liver firm	Is a	True	Abnormally hard consistency	Inferred relationship	Some
Endosteal hyperostoses	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Worth disease	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Syndrome with characteristics of congenital cerebellar hypoplasia, endosteal sclerosis, hypotonia, ataxia, mild to moderate developmental delay, short stature, hip dislocation, and tooth eruption disturbances. It has been described in four patients. Less common manifestations are microcephaly, strabismus, nystagmus, optic atrophy and dysarthria. It is appears to be transmitted as an autosomal recessive trait.	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Craniometadiaphyseal dysplasia	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Induratio penis plastica	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some	1
Lenz-Majewski hyperostosis syndrome	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Sclerosteosis	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Equine palatitis	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some	1
Osteochondrodysplasia with osteopetrosis	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Pulp stones	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some	1
Hyperphosphatasemia tarda	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Secondary dentin	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some	1
Cleidocranial dysostosis	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Abnormal hard tissue formation in pulp (disorder)	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some	1
Pyknodysostosis	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some
Abnormal pulp hard tissue NOS	Associated morphology	False	Abnormally hard consistency	Inferred relationship	Some	1

Reference Sets