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8757006: Hecht syndrome (disorder)

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

\Deformity (finding)\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Hecht syndrome
\Deformity (finding)\Congenital deformity\Arthrogryposis\Distal arthrogryposis syndrome\Hecht syndrome
\Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Hecht syndrome
\Deformity (finding)\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Hecht syndrome

\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Hecht syndrome
\Disease\Disorder of joint region\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Hecht syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Inherited arthrogryposis\Hecht syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Hecht syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Hecht syndrome
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital deformity\Arthrogryposis\Distal arthrogryposis syndrome\Hecht syndrome
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Inherited arthrogryposis\Hecht syndrome
\Disease\Movement disorder\Contracture of joint\Contracture of multiple joints\Arthrogryposis\Distal arthrogryposis syndrome\Hecht syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Inherited arthrogryposis\Hecht syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Inherited arthrogryposis\Hecht syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital deformity\Arthrogryposis\Distal arthrogryposis syndrome\Hecht 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
Hecht syndrome	Is a	Multiple malformation syndrome with unusual brain and/or neuromuscular findings	false	Inferred relationship	Some
Hecht syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Hecht syndrome	Finding site	Brain structure	false	Inferred relationship	Some	1
Hecht syndrome	Associated morphology	Congenital malformation	false	Inferred relationship	Some
Hecht syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Hecht syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	1
Hecht syndrome	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	1
Hecht syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Hecht syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Some
Hecht syndrome	Is a	Distal arthrogryposis syndrome	true	Inferred relationship	Some
Hecht syndrome	Is a	Inherited arthrogryposis	true	Inferred relationship	Some
Hecht syndrome	Interprets	Range of joint movement	true	Inferred relationship	Some	2
Hecht syndrome	Has interpretation	Decreased	true	Inferred relationship	Some	2
Hecht syndrome	Finding site	Structure of joint region	true	Inferred relationship	Some	1
Hecht syndrome	Associated morphology	Contracture	true	Inferred relationship	Some	1

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
15445015	Hecht syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
15446019	Trismus pseudocamptodactyly syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
830072015	Hecht syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5171587019	Distal arthrogryposis type 7	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5171588012	Dutch Kentucky syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5171589016	Hecht Beals syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5958501000172118	syndrome de Hecht	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4615341000172118	syndroom van Hecht	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4615351000172116	Dutch-Kentucky-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
4615361000172119	Hecht-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
4615371000172111	syndroom van trismus en pseudocamptodactylie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4615381000172114	TPS	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
4615391000172112	syndroom van kaakklem en pseudocamptodactylie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)