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1269226006: Spondylometaphyseal dysplasia, corneal dystrophy syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5183257011 Spondylometaphyseal dysplasia, corneal dystrophy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5183258018 Spondylometaphyseal dysplasia, corneal dystrophy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5400684017 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay with intellectual disability, postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, abnormalities of the spine, pelvis, and metaphyses, corneal clouding, and patent ductus arteriosus. Dysmorphic facial features include hypertelorism, prominent eyes, depressed nasal bridge, and short upturned nose. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400685016 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by developmental delay with intellectual disability, postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, abnormalities of the spine, pelvis, and metaphyses, corneal clouding, and patent ductus arteriosus. Dysmorphic facial features include hypertelorism, prominent eyes, depressed nasal bridge, and short upturned nose. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5183257011 Spondylometaphyseal dysplasia, corneal dystrophy syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5183258018 Spondylometaphyseal dysplasia, corneal dystrophy syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5183259014 A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay with intellectual disability, postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, abnormalities of the spine, pelvis and metaphyses, corneal clouding and patent ductus arteriosus. Dysmorphic facial features include hypertelorism, prominent eyes, depressed nasal bridge and short upturned nose. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400684017 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by developmental delay with intellectual disability, postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, abnormalities of the spine, pelvis, and metaphyses, corneal clouding, and patent ductus arteriosus. Dysmorphic facial features include hypertelorism, prominent eyes, depressed nasal bridge, and short upturned nose. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5400685016 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by developmental delay with intellectual disability, postnatal growth deficiency causing profound limb shortening with proximal and distal segments involvement, narrow chest, abnormalities of the spine, pelvis, and metaphyses, corneal clouding, and patent ductus arteriosus. Dysmorphic facial features include hypertelorism, prominent eyes, depressed nasal bridge, and short upturned nose. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
532131000274119 SMD-Hornhautdystrophie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
566881000274115 Spondylometaphysäre Dysplasie-Hornhautdystrophie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
532131000274119 SMD-Hornhautdystrophie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
566881000274115 Spondylometaphysäre Dysplasie-Hornhautdystrophie-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Is a Hereditary corneal dystrophy true Inferred relationship Existential restriction modifier (core metadata concept)
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Is a Spondylometaphyseal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 6
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Finding site Skeletal system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Finding site Limb structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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