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734173003: syndroom van skeletafwijking, cutis laxa, craniosynostose, ambigue geslachtsorganen, retardatie en afwijking van aangezicht (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3489209014 SCARF (skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489210016 SCARF syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3489211017 Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3489213019 Skeletal abnormality, cutis laxa, craniostenosis, ambiguous genitalia, retardation, facial abnormality syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6948551000146112 SCARF-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6948561000146110 syndroom van skeletafwijking, cutis laxa, craniosynostose, ambigue genitaliën, retardatie en afwijking van aangezicht nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12414931000146114 syndroom van skeletafwijking, cutis laxa, craniosynostose, ambigue geslachtsorganen, retardatie en afwijking van aangezicht (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
12414941000146118 syndroom van skeletafwijking, cutis laxa, craniosynostose, ambigue geslachtsorganen, retardatie en afwijking van aangezicht nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3489212012 Syndrome with the association of skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, psychomotor retardation and facial abnormalities. So far, it has been described in two males (maternal first cousins). The mode of inheritance was suggested to be X-linked recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
SCARF syndrome Is a Ambiguous genitalia true Inferred relationship Some
SCARF syndrome Is a Metabolic bone disease false Inferred relationship Some
SCARF syndrome Is a Craniosynostosis syndrome true Inferred relationship Some
SCARF syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
SCARF syndrome Is a mentale retardatie false Inferred relationship Some
SCARF syndrome Is a X-linked hereditary disease false Inferred relationship Some
SCARF syndrome Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
SCARF syndrome Is a Hereditary disorder of the integument false Inferred relationship Some
SCARF syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
SCARF syndrome Is a Reproductive system hereditary disorder true Inferred relationship Some
SCARF syndrome Is a Congenital/hereditary cutis laxa false Inferred relationship Some
SCARF syndrome Finding site Bone structure of cranium false Inferred relationship Some
SCARF syndrome Occurrence Congenital true Inferred relationship Some 5
SCARF syndrome Occurrence Congenital false Inferred relationship Some 6
SCARF syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 7
SCARF syndrome Occurrence Congenital false Inferred relationship Some 7
SCARF syndrome Occurrence Congenital false Inferred relationship Some 8
SCARF syndrome Associated morphology gebrekkige ontwikkeling (afwijkende morfologie) false Inferred relationship Some 5
SCARF syndrome Associated morphology congenitale premature fusie false Inferred relationship Some 6
SCARF syndrome Finding site Joint structure of suture of skull false Inferred relationship Some 6
SCARF syndrome Finding site Face structure false Inferred relationship Some 5
SCARF syndrome Finding site External genitalia structure false Inferred relationship Some 7
SCARF syndrome Finding site Skin structure false Inferred relationship Some 8
SCARF syndrome Is a Intellectual disability true Inferred relationship Some
SCARF syndrome Occurrence Congenital true Inferred relationship Some 2
SCARF syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
SCARF syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
SCARF syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
SCARF syndrome Occurrence Congenital true Inferred relationship Some 1
SCARF syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
SCARF syndrome Occurrence Congenital true Inferred relationship Some 3
SCARF syndrome Finding site External genitalia structure true Inferred relationship Some 2
SCARF syndrome Occurrence Congenital true Inferred relationship Some 4
SCARF syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
SCARF syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
SCARF syndrome Finding site Skin structure true Inferred relationship Some 1
SCARF syndrome Finding site Face structure true Inferred relationship Some 3
SCARF syndrome Associated morphology congenitale premature fusie false Inferred relationship Some 4
SCARF syndrome Finding site Joint structure of suture of skull true Inferred relationship Some 4
SCARF syndrome Finding site Connective tissue structure false Inferred relationship Some
SCARF syndrome Is a Musculoskeletal and connective tissue disorder (disorder) true Inferred relationship Some
SCARF syndrome Finding site Connective tissue structure true Inferred relationship Some 5
SCARF syndrome Is a Inherited cutis laxa (disorder) true Inferred relationship Some
SCARF syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
SCARF syndrome Is a X-linked recessive hereditary disease true Inferred relationship Some
SCARF syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 6
SCARF syndrome Has interpretation Impaired true Inferred relationship Some 6
SCARF syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 7
SCARF syndrome Has interpretation Impaired true Inferred relationship Some 7
SCARF syndrome Associated morphology Premature fusion true Inferred relationship Some 4
SCARF syndrome Is a Disorder involving the integument of fetus OR newborn true Inferred relationship Some
SCARF syndrome Is a Hereditary metabolic disease false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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