FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

290006: Melnick-Fraser syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2005. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
1568018 Melnick-Fraser syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1569014 Branchio-oto-renal syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
1570010 BOR syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
759766013 Melnick-Fraser syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Melnick-Fraser syndrome Is a Hereditary disorder of the urinary system false Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Renal disorders in inherited disease false Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Congenital anomaly of the kidney true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Multisystem disorder A-B false Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Finding site Urinary system structure false Inferred relationship Existential restriction modifier 9
Melnick-Fraser syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Finding site Kidney structure true Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Course Multiple superficial injuries of lower leg false Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Is a Congenital malformation of the urinary system false Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Finding site Kidney structure false Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Melnick-Fraser syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Melnick-Fraser syndrome Finding site Kidney structure false Inferred relationship Existential restriction modifier 2
Melnick-Fraser syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Melnick-Fraser syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Melnick-Fraser syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 3
Melnick-Fraser syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Melnick-Fraser syndrome Is a Hereditary nephropathy true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Melnick-Fraser syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Melnick-Fraser syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Melnick-Fraser syndrome Is a Congenital hearing disorder true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Developmental malformation of branchial arch true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Is a Hearing loss true Inferred relationship Existential restriction modifier
Melnick-Fraser syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Melnick-Fraser syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Melnick-Fraser syndrome Finding site Branchial arch structure true Inferred relationship Existential restriction modifier 5
Melnick-Fraser syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 5
Melnick-Fraser syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Melnick-Fraser syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Melnick-Fraser syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Melnick-Fraser syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Melnick-Fraser 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