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268262006: Acrocephalosyndactyly (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
400910012 Acrocephalosyndactyly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
660982014 Acrocephalosyndactyly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
81001000077112 acrocéphalosyndactylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
885581000172119 acro-céphalo-syndactylie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
999081000172119 ACS - acro-céphalo-syndactylie fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
651801000274119 Akrozephalosyndaktylie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


10 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acrocephalosyndactyly Is a Multisystem disorder A-B false Inferred relationship Some
Acrocephalosyndactyly Is a trouble multisytémique false Inferred relationship Some
Acrocephalosyndactyly Is a Multiple congenital malformations false Inferred relationship Some
Acrocephalosyndactyly Associated morphology Congenital malformation false Inferred relationship Some
Acrocephalosyndactyly Occurrence Congenital false Inferred relationship Some 3
Acrocephalosyndactyly Occurrence Congenital true Inferred relationship Some 2
Acrocephalosyndactyly Is a Congenital malformation syndrome (disorder) false Inferred relationship Some
Acrocephalosyndactyly Associated morphology anomalie du développement false Inferred relationship Some 1
Acrocephalosyndactyly Occurrence Congenital true Inferred relationship Some 1
Acrocephalosyndactyly Associated morphology Congenital premature fusion false Inferred relationship Some 2
Acrocephalosyndactyly Finding site Joint structure of suture of skull true Inferred relationship Some 2
Acrocephalosyndactyly Is a Craniosynostosis syndrome true Inferred relationship Some
Acrocephalosyndactyly Is a Syndactyly (disorder) true Inferred relationship Some
Acrocephalosyndactyly Finding site Bone structure of cranium false Inferred relationship Some
Acrocephalosyndactyly Associated morphology Congenital abnormal fusion false Inferred relationship Some 2
Acrocephalosyndactyly Finding site Digit structure false Inferred relationship Some 2
Acrocephalosyndactyly Associated morphology Congenital premature fusion false Inferred relationship Some 3
Acrocephalosyndactyly Finding site Joint structure of suture of skull false Inferred relationship Some 3
Acrocephalosyndactyly Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Acrocephalosyndactyly Associated morphology Congenital abnormal fusion false Inferred relationship Some 1
Acrocephalosyndactyly Finding site Digit structure true Inferred relationship Some 1
Acrocephalosyndactyly Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Acrocephalosyndactyly Is a Genetic disease true Inferred relationship Some
Acrocephalosyndactyly Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Acrocephalosyndactyly Associated morphology Premature fusion true Inferred relationship Some 2
Acrocephalosyndactyly Associated morphology Fusion that has occurred in a structure that is not normally fused. true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Acrocephalosyndactyly type I Is a True Acrocephalosyndactyly Inferred relationship Some
Acrocephalosyndactyly (Pfeiffer) Is a False Acrocephalosyndactyly Inferred relationship Some
Acrocephalopolysyndactyly Is a True Acrocephalosyndactyly Inferred relationship Some
Acrocephalosyndactyly type V (disorder) Is a True Acrocephalosyndactyly Inferred relationship Some
Craniosynostosis, Philadelphia type is a form of syndromic craniosynostosis, characterized by sagittal/dolichocephalic head shape with a relatively normal facial appearance and complete soft tissue syndactyly of hand and foot. Transmission is autosomal dominant with variable expression of the hand findings, and incomplete penetrance of the sagittal craniosynostosis. Craniosynostosis, Philadelphia type has been suggested to share the same etiology as syndactyly type 1A. Is a False Acrocephalosyndactyly Inferred relationship Some
Curry-Jones syndrome is a form of syndromic craniosynostosis characterized by unilateral coronal craniosynostosis or multiple suture synostosis associated with complete or partial agenesis of the corpus callosum, preaxial polysyndactyly and syndactyly of hands and/or feet, along with anomalies of the skin (characteristic pearly white areas that become scarred and atrophic, abnormal hair growth around the eyes and/or cheeks, and on the limbs), eyes (iris colobomas, microphthalmia,) and intestine (congenital short gut, malrotation, dysmotility, chronic constipation, bleeding and myofibromas). Developmental delay and variable degrees of intellectual disability may also be observed. Multiple intra-abdominal smooth muscle hamartomas, trichoblastoma of the skin, occipital meningoceles and development of desmoplastic medulloblastoma have been reported. Is a False Acrocephalosyndactyly Inferred relationship Some
Saethre-Chotzen syndrome Is a True Acrocephalosyndactyly Inferred relationship Some
syndrome de Summitt Is a False Acrocephalosyndactyly Inferred relationship Some
A polymalformative syndrome characterized by craniosynostosis, Poland anomaly, cranio-fronto-nasal dysplasia, and genital and breast anomalies. Is a False Acrocephalosyndactyly Inferred relationship Some
Jackson-Weiss syndrome Is a True Acrocephalosyndactyly Inferred relationship Some

This concept is not in any reference sets

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