FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.24 | FHIR Version n/a User: [n/a]

45167004: Moynahan's syndrome (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
syndrome de Moynahan	Is a	Ectodermal dysplasia with hair-tooth-nail-sweating defect	false	Inferred relationship	Some
syndrome de Moynahan	Is a	Congenital hamartosis	false	Inferred relationship	Some
syndrome de Moynahan	Occurrence	Congenital	false	Inferred relationship	Some
syndrome de Moynahan	Finding site	Skin structure	false	Inferred relationship	Some	1
syndrome de Moynahan	Associated morphology	Dysplasia	false	Inferred relationship	Some	1
syndrome de Moynahan	Associated morphology	Congenital anomaly	false	Inferred relationship	Some
syndrome de Moynahan	Associated morphology	Hamartoma	false	Inferred relationship	Some
syndrome de Moynahan	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
syndrome de Moynahan	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	1
syndrome de Moynahan	Finding site	Skin structure	false	Inferred relationship	Some	1
syndrome de Moynahan	Finding site	Skin structure	false	Inferred relationship	Some	2
syndrome de Moynahan	Is a	Congenital hamartoma (disorder)	false	Inferred relationship	Some
syndrome de Moynahan	Occurrence	Congenital	false	Inferred relationship	Some	2
syndrome de Moynahan	Finding site	Skin structure	false	Inferred relationship	Some	3
syndrome de Moynahan	Occurrence	Congenital	false	Inferred relationship	Some	3
syndrome de Moynahan	Associated morphology	Hamartoma	false	Inferred relationship	Some	3
syndrome de Moynahan	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	2
syndrome de Moynahan	Occurrence	Congenital	false	Inferred relationship	Some	4
syndrome de Moynahan	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	4
syndrome de Moynahan	Finding site	Ectoderm structure	false	Inferred relationship	Some	4
syndrome de Moynahan	Associated morphology	Hamartoma	false	Inferred relationship	Some	4
syndrome de Moynahan	Finding site	Structure of skin and/or mucous membrane (body structure)	false	Inferred relationship	Some	1
syndrome de Moynahan	Associated morphology	Lentigo (morphologic abnormality)	false	Inferred relationship	Some	1
syndrome de Moynahan	Is a	Lentiginosis (disorder)	false	Inferred relationship	Some
syndrome de Moynahan	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	2
syndrome de Moynahan	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	4
syndrome de Moynahan	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	3
syndrome de Moynahan	Finding site	Ectoderm structure	false	Inferred relationship	Some	2
syndrome de Moynahan	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	2
syndrome de Moynahan	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	3
syndrome de Moynahan	Associated morphology	Dysplasia	false	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
75318015	Moynahan's syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
75319011	Progressive cardiomyopathic lentiginosis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
782376016	Moynahan's syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
2842257014	Moynahan syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
946461000172115	syndrome de Moynahan	fr	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
980251000172114	syndrome d'alopécie, épilepsie, déficience intellectuelle	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
872641000172112	syndroom van Moynahan	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
930881000172114	alopecie, epilepsie, intellectuele achterstand-syndroom, Moynahan-type	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)