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773406003: Mandibular hypoplasia, deafness, progeroid syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3723420015 MDP (mandibular hypoplasia, deafness, progeroid) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3723421016 Mandibular hypoplasia, hearing loss, progeroid syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3723422011 Mandibular hypoplasia, deafness, progeroid syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3723423018 Mandibular hypoplasia, deafness, progeroid syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mandibular hypoplasia, deafness, progeroid syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Mandibular hypoplasia, deafness, progeroid syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Mandibular hypoplasia, deafness, progeroid syndrome Is a Congenital micrognathism true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Is a Metabolic bone disease true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Mandibular hypoplasia, deafness, progeroid syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier 1
Mandibular hypoplasia, deafness, progeroid syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Mandibular hypoplasia, deafness, progeroid syndrome Is a Premature aging syndrome true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Mandibular hypoplasia, deafness, progeroid syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Mandibular hypoplasia, deafness, progeroid syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Mandibular hypoplasia, deafness, progeroid syndrome Finding site Bone structure of mandible true Inferred relationship Existential restriction modifier 1
Mandibular hypoplasia, deafness, progeroid syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Mandibular hypoplasia, deafness, progeroid syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 5
Mandibular hypoplasia, deafness, progeroid syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 5
Mandibular hypoplasia, deafness, progeroid syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 5
Mandibular hypoplasia, deafness, progeroid syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Mandibular hypoplasia, deafness, progeroid syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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