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766870005: Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (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
3662960019 Finucane Kurtz Scott syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3662961015 Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3662962010 Epiphyseal dysplasia, hearing loss, dysmorphism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3664260010 A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Severe behaviour disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns are also associated. There have been no further descriptions in the literature since 1992. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3664261014 A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of developmental delay, intellectual disability, short stature, sensorineural hearing impairment, facial dysmorphism (including epicanthus, broad, depressed nasal bridge, broad, fleshy nasal tip, mildly anteverted nares, deep nasolabial folds, broad mouth with thin upper lip) and skeletal anomalies (including abnormally placed thumbs, brachydactyly, scoliosis, dysplastic carpal bones). Severe behavior disturbances (aggression, hyperactivity), as well as hypopigmented skin lesions and hypoplastic digital patterns are also associated. There have been no further descriptions in the literature since 1992. 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
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Associated morphology dysgenese false Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Hearing loss associated with syndrome true Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Finding site Face structure true Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Sensorineural hearing loss false Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Interprets træk vedr. funktion false Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Epiphyseal dysplasia true Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Congenital hearing disorder false Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Interprets Hearing true Inferred relationship Some 5
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Associated morphology kongenit dysplasi false Inferred relationship Some 2
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Associated morphology dysgenese false Inferred relationship Some 4
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Finding site Structure of epiphysis true Inferred relationship Some 2
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Finding site Ear structure true Inferred relationship Some 1
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Finding site Limb structure true Inferred relationship Some 4
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Chronic mental disorder false Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Chronic disease of ear false Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Congenital sensorineural hearing loss (disorder) true Inferred relationship Some
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 6
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 7
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 7
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 8
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 8
Epiphyseal dysplasia, hearing loss, dysmorphism syndrome (disorder) Is a Chronic deafness true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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