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763837007: Oro-facial digital syndrome type 14 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3644670013 Oro-facial digital syndrome type 14 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644671012 Oro-facial digital syndrome type 14 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644672017 Microcephaly, cerebral malformation, orofaciodigital syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644673010 Orofaciodigital syndrome type 14 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5404234012 Orofaciodigital syndrome type 14 is a rare subtype of orofaciodigital syndrome, with autosomal recessive inheritance and C2CD3 mutations, characterized by severe microcephaly, trigonocephaly, severe intellectual disability and micropenis, in addition to oral, facial and digital malformations (gingival frenulae, lingual hamartomas, cleft/lobulated tongue, cleft palate, telecanthus, up-slanting palpebral fissures, microretrognathia, postaxial polydactyly of hands and duplication of hallux). Corpus callosum agenesis and vermis hypoplasia with molar tooth sign, on brain imaging, are also associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404235013 Orofaciodigital syndrome type 14 is a rare subtype of orofaciodigital syndrome, with autosomal recessive inheritance and C2CD3 mutations, characterised by severe microcephaly, trigonocephaly, severe intellectual disability and micropenis, in addition to oral, facial and digital malformations (gingival frenulae, lingual hamartomas, cleft/lobulated tongue, cleft palate, telecanthus, up-slanting palpebral fissures, microretrognathia, postaxial polydactyly of hands and duplication of hallux). Corpus callosum agenesis and vermis hypoplasia with molar tooth sign, on brain imaging, are also associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3644670013 Oro-facial digital syndrome type 14 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644671012 Oro-facial digital syndrome type 14 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644672017 Microcephaly, cerebral malformation, orofaciodigital syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3644673010 Orofaciodigital syndrome type 14 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664245012 A rare subtype of orofaciodigital syndrome, with autosomal recessive inheritance and C2CD3 mutations. The disease has characteristics of severe microcephaly, trigonocephaly, severe intellectual disability and micropenis, in addition to oral, facial and digital malformations (gingival frenulum, lingual hamartomas, cleft/lobulated tongue, cleft palate, telecanthus, up-slanting palpebral fissures, microretrognathia, postaxial polydactyly of hands and duplication of hallux). Corpus callosum agenesis and vermis hypoplasia with molar tooth sign on brain imaging are also associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404234012 Orofaciodigital syndrome type 14 is a rare subtype of orofaciodigital syndrome, with autosomal recessive inheritance and C2CD3 mutations, characterized by severe microcephaly, trigonocephaly, severe intellectual disability and micropenis, in addition to oral, facial and digital malformations (gingival frenulae, lingual hamartomas, cleft/lobulated tongue, cleft palate, telecanthus, up-slanting palpebral fissures, microretrognathia, postaxial polydactyly of hands and duplication of hallux). Corpus callosum agenesis and vermis hypoplasia with molar tooth sign, on brain imaging, are also associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404235013 Orofaciodigital syndrome type 14 is a rare subtype of orofaciodigital syndrome, with autosomal recessive inheritance and C2CD3 mutations, characterised by severe microcephaly, trigonocephaly, severe intellectual disability and micropenis, in addition to oral, facial and digital malformations (gingival frenulae, lingual hamartomas, cleft/lobulated tongue, cleft palate, telecanthus, up-slanting palpebral fissures, microretrognathia, postaxial polydactyly of hands and duplication of hallux). Corpus callosum agenesis and vermis hypoplasia with molar tooth sign, on brain imaging, are also associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3418701001000113 Oro-fazio-digitales Syndrom Typ 14 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6485931000241111 syndrome oro-facio-digital, microcéphalie et malformation cérébrale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6485941000241118 OFD14 - syndrome oro-facio-digital de type 14 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6485951000241115 syndrome oro-facio-digital de type 14 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6485931000241111 syndrome oro-facio-digital, microcéphalie et malformation cérébrale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6485941000241118 OFD14 - syndrome oro-facio-digital de type 14 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6485951000241115 syndrome oro-facio-digital de type 14 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3418701001000113 Oro-fazio-digitales Syndrom Typ 14 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
Oro-facial digital syndrome type 14 (disorder) Is a microcéphalie false Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Oral-facial-digital syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Finding site Ectoderm structure true Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 14 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Oro-facial digital syndrome type 14 (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Oro-facial digital syndrome type 14 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Oro-facial digital syndrome type 14 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 5
Oro-facial digital syndrome type 14 (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 5
Oro-facial digital syndrome type 14 (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Oro-facial digital syndrome type 14 (disorder) Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 4
Oro-facial digital syndrome type 14 (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 14 (disorder) Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 14 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 5
Oro-facial digital syndrome type 14 (disorder) Finding site Ectoderm structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Oro-facial digital syndrome type 14 (disorder) Finding site Digit structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 14 (disorder) Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Finding site Structure of internal part of mouth true Inferred relationship Existential restriction modifier (core metadata concept) 3
Oro-facial digital syndrome type 14 (disorder) Finding site Digit structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Oro-facial digital syndrome type 14 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Oro-facial digital syndrome type 14 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Oro-facial digital syndrome type 14 (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Oro-facial digital syndrome type 14 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Oro-facial digital syndrome type 14 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 14 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 14 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Oro-facial digital syndrome type 14 (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 5
Oro-facial digital syndrome type 14 (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 6
Oro-facial digital syndrome type 14 (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Interprets Birth head circumference true Inferred relationship Existential restriction modifier (core metadata concept) 7
Oro-facial digital syndrome type 14 (disorder) Finding site Head structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Oro-facial digital syndrome type 14 (disorder) Has interpretation Below reference range true Inferred relationship Existential restriction modifier (core metadata concept) 7
Oro-facial digital syndrome type 14 (disorder) Is a Congenital microcephaly (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Oro-facial digital syndrome type 14 (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 8
Oro-facial digital syndrome type 14 (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 8
Oro-facial digital syndrome type 14 (disorder) Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 9
Oro-facial digital syndrome type 14 (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 9
Oro-facial digital syndrome type 14 (disorder) Associated morphology Abnormal smallness (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 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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