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722105002: Oro-facial digital syndrome type 5 (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330477018 Oro-facial digital syndrome type 5 (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3330480017 Oro-facial digital syndrome type 5 en Synonym Active Case insensitive SNOMED CT core
3330708014 Orofaciodigital syndrome type 5 en Synonym Active Case insensitive SNOMED CT core
3330709018 Orofaciodigital syndrome Thurston type en Synonym Active Initial character case insensitive SNOMED CT core
3330710011 Thurston syndrome en Synonym Active Case sensitive SNOMED CT core
3330711010 Syndrome with characteristics of median cleft of upper lip, postaxial polydactyly of hands and feet and oral manifestations (duplicated frenulum). Less than 20 patients (predominantly of Indian origin) have been reported so far. Autosomal recessive inheritance has been suggested, but the causative gene has not yet been identified. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Orofaciodigital syndrome type 5 Finding site Face structure true Inferred relationship Some 2
Orofaciodigital syndrome type 5 Associated morphology Morphologically abnormal structure true Inferred relationship Some 3
Orofaciodigital syndrome type 5 Pathological process Pathological developmental process true Inferred relationship Some 3
Orofaciodigital syndrome type 5 Pathological process Pathological developmental process true Inferred relationship Some 4
Orofaciodigital syndrome type 5 Pathological process Pathological developmental process true Inferred relationship Some 5
Orofaciodigital syndrome type 5 Pathological process Pathological developmental process true Inferred relationship Some 2
Orofaciodigital syndrome type 5 Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Orofaciodigital syndrome type 5 Associated morphology Morphologically abnormal structure true Inferred relationship Some 4
Orofaciodigital syndrome type 5 Pathological process Pathological developmental process true Inferred relationship Some 1
Orofaciodigital syndrome type 5 Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Orofaciodigital syndrome type 5 Associated morphology Dysplasia true Inferred relationship Some 5
Orofaciodigital syndrome type 5 Is a Developmental hereditary disorder true Inferred relationship Some
Orofaciodigital syndrome type 5 Interprets Intellectual ability true Inferred relationship Some 6
Orofaciodigital syndrome type 5 Has interpretation Impaired true Inferred relationship Some 6
Orofaciodigital syndrome type 5 Interprets Adaptation behaviour true Inferred relationship Some 7
Orofaciodigital syndrome type 5 Has interpretation Impaired true Inferred relationship Some 7
Orofaciodigital syndrome type 5 Is a Oral-facial-digital syndrome true Inferred relationship Some
Orofaciodigital syndrome type 5 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Orofaciodigital syndrome type 5 Is a Intellectual disability false Inferred relationship Some
Orofaciodigital syndrome type 5 Is a Hereditary disorder of the integument true Inferred relationship Some
Orofaciodigital syndrome type 5 Associated morphology Developmental abnormality false Inferred relationship Some 4
Orofaciodigital syndrome type 5 Occurrence Congenital true Inferred relationship Some 4
Orofaciodigital syndrome type 5 Finding site Face structure false Inferred relationship Some 4
Orofaciodigital syndrome type 5 Associated morphology Congenital dysplasia false Inferred relationship Some 5
Orofaciodigital syndrome type 5 Occurrence Congenital true Inferred relationship Some 5
Orofaciodigital syndrome type 5 Finding site Ectoderm structure true Inferred relationship Some 5
Orofaciodigital syndrome type 5 Associated morphology Developmental abnormality false Inferred relationship Some 6
Orofaciodigital syndrome type 5 Occurrence Congenital false Inferred relationship Some 6
Orofaciodigital syndrome type 5 Occurrence Congenital false Inferred relationship Some 7
Orofaciodigital syndrome type 5 Finding site Skin structure true Inferred relationship Some 4
Orofaciodigital syndrome type 5 Associated morphology Developmental abnormality false Inferred relationship Some 5
Orofaciodigital syndrome type 5 Finding site Limb structure false Inferred relationship Some 6
Orofaciodigital syndrome type 5 Associated morphology Congenital dysplasia false Inferred relationship Some 7
Orofaciodigital syndrome type 5 Finding site Ectoderm structure false Inferred relationship Some 7
Orofaciodigital syndrome type 5 Finding site Skin structure false Inferred relationship Some 5
Orofaciodigital syndrome type 5 Is a Intellectual disability true Inferred relationship Some
Orofaciodigital syndrome type 5 Is a Digestive system hereditary disorder true Inferred relationship Some
Orofaciodigital syndrome type 5 Occurrence Congenital true Inferred relationship Some 1
Orofaciodigital syndrome type 5 Associated morphology Developmental abnormality false Inferred relationship Some 2
Orofaciodigital syndrome type 5 Occurrence Congenital true Inferred relationship Some 2
Orofaciodigital syndrome type 5 Finding site Structure of internal part of mouth true Inferred relationship Some 1
Orofaciodigital syndrome type 5 Finding site Digit structure false Inferred relationship Some 2
Orofaciodigital syndrome type 5 Associated morphology Developmental abnormality false Inferred relationship Some 3
Orofaciodigital syndrome type 5 Occurrence Congenital true Inferred relationship Some 3
Orofaciodigital syndrome type 5 Finding site Digit structure true Inferred relationship Some 3
Orofaciodigital syndrome type 5 Finding site Structure of internal part of mouth false Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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