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722056009: Oculocerebrofacial syndrome Kaufman type (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
3330409019 Oculocerebrofacial syndrome Kaufman type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330410012 Oculocerebrofacial syndrome Kaufman type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330411011 Kaufman oculocerebrofacial syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402799017 A rare, genetic, syndromic intellectual disability characterized by severe intellectual disability, distinctive craniofacial features and variable multiple congenital anomalies including ocular, brain, urogenital and skeletal abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402800018 A rare, genetic, syndromic intellectual disability characterised by severe intellectual disability, distinctive craniofacial features and variable multiple congenital anomalies including ocular, brain, urogenital and skeletal abnormalities. 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
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Microcephalus false Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Congenital anomaly of eye true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Congenital anomaly of brain false Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Mental retardation false Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Hereditary disorder of nervous system false Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Associated morphology Congenital smallness false Inferred relationship Some 3
Oculocerebrofacial syndrome Kaufman type (disorder) Occurrence Congenital true Inferred relationship Some 3
Oculocerebrofacial syndrome Kaufman type (disorder) Finding site Brain structure false Inferred relationship Some 3
Oculocerebrofacial syndrome Kaufman type (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 4
Oculocerebrofacial syndrome Kaufman type (disorder) Occurrence Congenital false Inferred relationship Some 4
Oculocerebrofacial syndrome Kaufman type (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 5
Oculocerebrofacial syndrome Kaufman type (disorder) Occurrence Congenital false Inferred relationship Some 5
Oculocerebrofacial syndrome Kaufman type (disorder) Finding site Eye structure false Inferred relationship Some 4
Oculocerebrofacial syndrome Kaufman type (disorder) Finding site Face structure false Inferred relationship Some 5
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Intellectual disability true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Occurrence Congenital true Inferred relationship Some 1
Oculocerebrofacial syndrome Kaufman type (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Oculocerebrofacial syndrome Kaufman type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oculocerebrofacial syndrome Kaufman type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Oculocerebrofacial syndrome Kaufman type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oculocerebrofacial syndrome Kaufman type (disorder) Occurrence Congenital true Inferred relationship Some 2
Oculocerebrofacial syndrome Kaufman type (disorder) Finding site Eye structure true Inferred relationship Some 2
Oculocerebrofacial syndrome Kaufman type (disorder) Finding site Face structure true Inferred relationship Some 1
Oculocerebrofacial syndrome Kaufman type (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Finding site Head structure true Inferred relationship Some 3
Oculocerebrofacial syndrome Kaufman type (disorder) Has interpretation Below reference range true Inferred relationship Some 4
Oculocerebrofacial syndrome Kaufman type (disorder) Interprets Birth head circumference true Inferred relationship Some 4
Oculocerebrofacial syndrome Kaufman type (disorder) Is a Congenital microcephaly (disorder) true Inferred relationship Some
Oculocerebrofacial syndrome Kaufman type (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 5
Oculocerebrofacial syndrome Kaufman type (disorder) Has interpretation Impaired true Inferred relationship Some 5
Oculocerebrofacial syndrome Kaufman type (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 6
Oculocerebrofacial syndrome Kaufman type (disorder) Has interpretation Impaired true Inferred relationship Some 6
Oculocerebrofacial syndrome Kaufman type (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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