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722065002: Okamoto 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
3330445016 Okamoto syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330446015 Okamoto syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330447012 Okamoto syndrome is characterised by congenital hydronephrosis, intellectual deficit, growth retardation, cleft palate, generalised hypotonia and a characteristic face. Cardiac anomalies have also been reported. To date, 6 cases have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330448019 Okamoto syndrome is characterized by congenital hydronephrosis, intellectual deficit, growth retardation, cleft palate, generalized hypotonia and a characteristic face. Cardiac anomalies have also been reported. To date, 6 cases have been reported. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3906731000052112 Okamotos syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Okamoto syndrome (disorder) Is a Congenital hydronephrosis true Inferred relationship Some
Okamoto syndrome (disorder) Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Okamoto syndrome (disorder) Is a Cleft palate true Inferred relationship Some
Okamoto syndrome (disorder) Is a mental retardation false Inferred relationship Some
Okamoto syndrome (disorder) Is a Growth retardation (disorder) true Inferred relationship Some
Okamoto syndrome (disorder) Occurrence Congenital false Inferred relationship Some 5
Okamoto syndrome (disorder) Associated morphology kongenital dilatation false Inferred relationship Some 7
Okamoto syndrome (disorder) Occurrence Congenital false Inferred relationship Some 7
Okamoto syndrome (disorder) Finding site Kidney structure false Inferred relationship Some 7
Okamoto syndrome (disorder) Associated morphology Obstruction false Inferred relationship Some 8
Okamoto syndrome (disorder) Finding site Renal collecting system structure false Inferred relationship Some 8
Okamoto syndrome (disorder) Occurrence Congenital false Inferred relationship Some 6
Okamoto syndrome (disorder) Finding site Renal collecting system structure false Inferred relationship Some 9
Okamoto syndrome (disorder) Associated morphology medfödd utebliven fusion false Inferred relationship Some 6
Okamoto syndrome (disorder) Finding site Palatal structure false Inferred relationship Some 6
Okamoto syndrome (disorder) Associated morphology utvecklingsabnormitet false Inferred relationship Some 5
Okamoto syndrome (disorder) Finding site Face structure false Inferred relationship Some 5
Okamoto syndrome (disorder) Associated morphology Dilatation false Inferred relationship Some 9
Okamoto syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 1
Okamoto syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Okamoto syndrome (disorder) Finding site Palatal structure false Inferred relationship Some 1
Okamoto syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
Okamoto syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Okamoto syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Okamoto syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Okamoto syndrome (disorder) Finding site Face structure true Inferred relationship Some 3
Okamoto syndrome (disorder) Finding site Kidney structure false Inferred relationship Some 1
Okamoto syndrome (disorder) Finding site Palatal structure true Inferred relationship Some 2
Okamoto syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Okamoto syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Okamoto syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 2
Okamoto syndrome (disorder) Associated morphology kongenital dilatation false Inferred relationship Some 1
Okamoto syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Okamoto syndrome (disorder) Associated morphology Dilatation true Inferred relationship Some 1
Okamoto syndrome (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 4
Okamoto syndrome (disorder) Associated morphology Obstruction false Inferred relationship Some 4
Okamoto syndrome (disorder) Finding site Renal collecting system structure false Inferred relationship Some 4
Okamoto syndrome (disorder) Finding site Renal collecting system structure true Inferred relationship Some 1
Okamoto syndrome (disorder) Occurrence Congenital false Inferred relationship Some 4
Okamoto syndrome (disorder) Finding site Bone structure of head false Inferred relationship Some 4
Okamoto syndrome (disorder) Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 4
Okamoto syndrome (disorder) Associated morphology Growth retardation true Inferred relationship Some 5
Okamoto syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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