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783097004: Stickler syndrome type 3 (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3757572012 Stickler syndrome non-ocular type en Synonym Active Case sensitive SNOMED CT core
3757573019 Stickler syndrome type 3 (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3757574013 Stickler syndrome type 3 en Synonym Active Case sensitive SNOMED CT core
4945009011 Autosomal dominant otospondylomegaepiphyseal dysplasia en Synonym Active Case insensitive SNOMED CT core
4945010018 AD OSMED - autosomal dominant otospondylomegaepiphyseal dysplasia en Synonym Active Case sensitive SNOMED CT core
3757575014 A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of craniofacial dysmorphism (midface hypoplasia, depressed nasal bridge, small nose with upturned tip, cleft palate, Pierre Robin sequence), bilateral, pronounced sensorineural hearing loss and skeletal/joint anomalies (including spondyloepiphyseal dysplasia, arthralgia/arthropathy), in the absence of ocular abnormalities. There is evidence the disease is caused by heterozygous mutation in the COL11A2 gene on chromosome 6p21. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Stickler syndrome type 3 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Stickler syndrome type 3 Is a Hearing loss associated with syndrome true Inferred relationship Some
Stickler syndrome type 3 Occurrence Congenital true Inferred relationship Some 2
Stickler syndrome type 3 Is a Spondyloepiphyseal dysplasia congenita true Inferred relationship Some
Stickler syndrome type 3 Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Stickler syndrome type 3 Pathological process Pathological developmental process true Inferred relationship Some 1
Stickler syndrome type 3 Associated morphology Dysplasia true Inferred relationship Some 1
Stickler syndrome type 3 Occurrence Congenital true Inferred relationship Some 1
Stickler syndrome type 3 Finding site Bone structure true Inferred relationship Some 1
Stickler syndrome type 3 Occurrence Congenital true Inferred relationship Some 3
Stickler syndrome type 3 Is a Congenital sensorineural hearing loss true Inferred relationship Some
Stickler syndrome type 3 Is a Auditory system hereditary disorder true Inferred relationship Some
Stickler syndrome type 3 Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Stickler syndrome type 3 Finding site Ear structure false Inferred relationship Some 3
Stickler syndrome type 3 Finding site Face structure true Inferred relationship Some 2
Stickler syndrome type 3 Pathological process Pathological developmental process true Inferred relationship Some 2
Stickler syndrome type 3 Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Stickler syndrome type 3 Interprets Hearing true Inferred relationship Some 4
Stickler syndrome type 3 Is a Disorder of ear false Inferred relationship Some
Stickler syndrome type 3 Is a Developmental hereditary disorder true Inferred relationship Some
Stickler syndrome type 3 Is a Decreased hearing true Inferred relationship Some
Stickler syndrome type 3 Has interpretation Decreased true Inferred relationship Some 4
Stickler syndrome type 3 Finding site Structure of auditory system true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

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