FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

720418008: Acrocraniofacial dysostosis (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
3320697013 Acrocraniofacial dysostosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3320698015 Acrocraniofacial dysostosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3320699011 Kaplan Plauchu Fitch syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402324018 A very rare acrofacial dysostosis characterized by short stature, acrocephaly, ocular hypertelorism, ptosis of eyelids, ocular proptosis, downslanting palpebral fissures, high nasal bridge, anteverted nostrils, short philtrum, cleft palate, micrognathia, abnormal external ears, preauricular pits, mixed hearing loss, bulbous digits, metatarsus varus, pectus excavatum and various radiological abnormalities. Features of this syndrome were reported to overlap with otopalatodigital syndrome types 1 and 2. There have been no further descriptions in the literature since 1988. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402325017 A very rare acrofacial dysostosis characterised by short stature, acrocephaly, ocular hypertelorism, ptosis of eyelids, ocular proptosis, downslanting palpebral fissures, high nasal bridge, anteverted nostrils, short philtrum, cleft palate, micrognathia, abnormal external ears, preauricular pits, mixed hearing loss, bulbous digits, metatarsus varus, pectus excavatum and various radiological abnormalities. Features of this syndrome were reported to overlap with otopalatodigital syndrome types 1 and 2. There have been no further descriptions in the literature since 1988. 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
Acrocraniofacial dysostosis (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Acrocraniofacial dysostosis (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Acrocraniofacial dysostosis (disorder) Is a Dysostosis of bone of skull true Inferred relationship Some
Acrocraniofacial dysostosis (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Acrocraniofacial dysostosis (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Acrocraniofacial dysostosis (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Occurrence Congenital true Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Finding site Bone structure of cranium true Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Occurrence Congenital false Inferred relationship Some 4
Acrocraniofacial dysostosis (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 5
Acrocraniofacial dysostosis (disorder) Occurrence Congenital false Inferred relationship Some 5
Acrocraniofacial dysostosis (disorder) Finding site Face structure false Inferred relationship Some 5
Acrocraniofacial dysostosis (disorder) Associated morphology Developmental anomaly false Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Finding site Limb structure false Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 4
Acrocraniofacial dysostosis (disorder) Finding site Bone structure of cranium false Inferred relationship Some 4
Acrocraniofacial dysostosis (disorder) Occurrence Congenital true Inferred relationship Some 2
Acrocraniofacial dysostosis (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Acrocraniofacial dysostosis (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Acrocraniofacial dysostosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Acrocraniofacial dysostosis (disorder) Occurrence Congenital true Inferred relationship Some 1
Acrocraniofacial dysostosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Acrocraniofacial dysostosis (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Finding site Face structure true Inferred relationship Some 2
Acrocraniofacial dysostosis (disorder) Finding site Limb structure true Inferred relationship Some 1
Acrocraniofacial dysostosis (disorder) Associated morphology Dysplasia true Inferred relationship Some 3
Acrocraniofacial dysostosis (disorder) Is a Developmental hereditary disorder true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

Back to Start