FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

74370006: Micromelia (disorder)

Status: current, Defined. Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
123510010 Micromelia en Synonym Active Case insensitive SNOMED CT core
123512019 Micromelus en Synonym Active Case insensitive SNOMED CT core
123513012 Micromelic dwarf en Synonym Active Case insensitive SNOMED CT core
123515017 Nanomelia en Synonym Active Case insensitive SNOMED CT core
814861012 Micromelia (disorder) en Fully specified name Active Case insensitive SNOMED CT core

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Micromelia Pathological process Pathological developmental process true Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Is a Longitudinal deficiency of limb false Inferred relationship Some
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Associated morphology Congenital smallness true Inferred relationship Some 1
Micromelia Occurrence Congenital false Inferred relationship Some 2
Micromelia Finding site Limb structure false Inferred relationship Some 2
Micromelia Associated morphology Abnormally short growth false Inferred relationship Some 2
Micromelia Occurrence Congenital false Inferred relationship Some 3
Micromelia Associated morphology Abnormal shortening false Inferred relationship Some 3
Micromelia Finding site Limb structure false Inferred relationship Some 3
Micromelia Associated morphology Abnormal shortening false Inferred relationship Some 2
Micromelia Is a Congenital anomaly of limb true Inferred relationship Some
Micromelia Finding site Entire limb false Inferred relationship Some 2
Micromelia Associated morphology Congenital smallness false Inferred relationship Some 4
Micromelia Occurrence Congenital false Inferred relationship Some 4
Micromelia Finding site Limb structure false Inferred relationship Some 4
Micromelia Occurrence Congenital true Inferred relationship Some 1
Micromelia Finding site Entire limb true Inferred relationship Some 1
Micromelia Finding site Limb structure false Inferred relationship Some 1
Micromelia Associated morphology Developmental abnormality false Inferred relationship Some
Micromelia Associated morphology Congenital smallness false Inferred relationship Some 1
Micromelia Associated morphology Abnormally short growth false Inferred relationship Some 2
Micromelia Finding site Musculoskeletal structure of limb false Inferred relationship Some
Micromelia Occurrence Congenital false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Diastrophic dysplasia Is a True Micromelia Inferred relationship Some
Micromelic dwarfism Fryn type Is a True Micromelia Inferred relationship Some
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome Is a True Micromelia Inferred relationship Some
Microlissencephaly micromelia syndrome Is a True Micromelia Inferred relationship Some
Short rib polydactyly syndrome Saldino Noonan type Is a True Micromelia Inferred relationship Some
Polyneuropathy, intellectual disability, acromicria, premature menopause syndrome Is a True Micromelia Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start