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720565000: Bohring Opitz syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3321255015 Bohring Opitz syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321256019 Bohring Opitz syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321257011 C-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321258018 Opitz trigonocephaly-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321259014 Bohring syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402399015 A rare multiple congenital anomalies syndrome characterized by intrauterine growth retardation (IUGR), postnatal failure to thrive, severe feeding difficulties, microcephaly/trigonocephaly, facial dysmorphism, a recognizable upper limb posture and severe developmental delay. The upper limb posture consists of internal rotation of the shoulders, flexion of the elbows, ulnar deviation of wrists and/or metacarpophalangeal joints. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402400010 A rare multiple congenital anomalies syndrome characterised by intrauterine growth retardation (IUGR), postnatal failure to thrive, severe feeding difficulties, microcephaly/trigonocephaly, facial dysmorphism, a recognisable upper limb posture and severe developmental delay. The upper limb posture consists of internal rotation of the shoulders, flexion of the elbows, ulnar deviation of wrists and/or metacarpophalangeal joints. 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
Bohring Opitz syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Bohring Opitz syndrome (disorder) Is a Developmental delay true Inferred relationship Some
Bohring Opitz syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Finding site Limb structure true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Bohring Opitz syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Bohring Opitz syndrome (disorder) Finding site Face structure false Inferred relationship Some 3
Bohring Opitz syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Bohring Opitz syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Bohring Opitz syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Bohring Opitz syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Bohring Opitz syndrome (disorder) Finding site Face structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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