FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

702362004: Craniofacial deafness hand syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2995560012 Craniofacial deafness hand syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995823017 Craniofacial deafness hand syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3881249013 Sommer Young Wee Frye syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Craniofacial deafness hand syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Craniofacial deafness hand syndrome Is a Multisystem disorder false Inferred relationship Existential restriction modifier
Craniofacial deafness hand syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Craniofacial deafness hand syndrome Is a Congenital anomaly of hand true Inferred relationship Existential restriction modifier
Craniofacial deafness hand syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Craniofacial deafness hand syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Craniofacial deafness hand syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Craniofacial deafness hand syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Craniofacial deafness hand syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Craniofacial deafness hand syndrome Finding site Hand structure true Inferred relationship Existential restriction modifier 1
Craniofacial deafness hand syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Craniofacial deafness hand syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Craniofacial deafness hand syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Craniofacial deafness hand syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Craniofacial deafness hand syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Craniofacial deafness hand syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Craniofacial deafness hand syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Craniofacial deafness hand syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Craniofacial deafness hand 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

Back to Start