FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

722383001: Catel Manzke syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3331772015 Catel Manzke syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3331773013 Catel Manzke syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3331776017 Micrognathia digital syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3331777014 Palatodigital syndrome Catel-Manzke type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Catel Manzke syndrome Is a Congenital anomaly of finger true Inferred relationship Existential restriction modifier
Catel Manzke syndrome Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier
Catel Manzke syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Catel Manzke syndrome Is a Dysostosis true Inferred relationship Existential restriction modifier
Catel Manzke syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Catel Manzke syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Catel Manzke syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Catel Manzke syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Catel Manzke syndrome Finding site Index finger structure true Inferred relationship Existential restriction modifier 2
Catel Manzke syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 3
Catel Manzke syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Catel Manzke syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 3
Catel Manzke syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Catel Manzke syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Catel Manzke syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Catel Manzke syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Catel Manzke syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Catel Manzke syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Catel Manzke syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Catel Manzke 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