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720429007: Acrofacial dysostosis Palagonia 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
3320728018 Acrofacial dysostosis Palagonia type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3320729014 Acrofacial dysostosis Palagonia type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5402329011 A rare acrofacial dysostosis characterized by normal intelligence, shortness of stature, and mild acrofacial dysostosis (malar hypoplasia, micrognathia and webbing of digits with shortening of the fourth metacarpals) associated with oligodontia, normal or high arched palate, aplasia cutis verticis with pili torti, mild cutaneous syndactyly of digits 2-5, and unilateral cleft lip. Features are similar to those seen in Zlotogora-Ogur syndrome, although the latter shows no sign of acrofacial dysostosis. There have been no further reports in the literature since 1997. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402330018 A rare acrofacial dysostosis characterised by normal intelligence, shortness of stature, and mild acrofacial dysostosis (malar hypoplasia, micrognathia and webbing of digits with shortening of the fourth metacarpals) associated with oligodontia, normal or high arched palate, aplasia cutis verticis with pili torti, mild cutaneous syndactyly of digits 2-5, and unilateral cleft lip. Features are similar to those seen in Zlotogora-Ogur syndrome, although the latter shows no sign of acrofacial dysostosis. There have been no further reports in the literature since 1997. 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
Acrofacial dysostosis Palagonia type (disorder) Finding site Bone structure of face true Inferred relationship Some 2
Acrofacial dysostosis Palagonia type (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Is a Congenital anomaly of face bones true Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Is a Dysostosis true Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Acrofacial dysostosis Palagonia type (disorder) Occurrence Congenital true Inferred relationship Some 2
Acrofacial dysostosis Palagonia type (disorder) Finding site Bone structure of extremity false Inferred relationship Some 2
Acrofacial dysostosis Palagonia type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 3
Acrofacial dysostosis Palagonia type (disorder) Occurrence Congenital false Inferred relationship Some 3
Acrofacial dysostosis Palagonia type (disorder) Finding site Bone structure of extremity false Inferred relationship Some 3
Acrofacial dysostosis Palagonia type (disorder) Is a Lesion of face true Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Acrofacial dysostosis Palagonia type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Acrofacial dysostosis Palagonia type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Acrofacial dysostosis Palagonia type (disorder) Finding site Bone structure of face false Inferred relationship Some 1
Acrofacial dysostosis Palagonia type (disorder) Occurrence Congenital true Inferred relationship Some 1
Acrofacial dysostosis Palagonia type (disorder) Finding site Bone structure of extremity true Inferred relationship Some 1
Acrofacial dysostosis Palagonia type (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Acrofacial dysostosis Palagonia type (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Acrofacial dysostosis Palagonia type (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Acrofacial dysostosis Palagonia type (disorder) Is a Congenital dysplasia of limb (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)

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