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

783143001: Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3757821010 Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia en Synonym Active Entire term case sensitive SNOMED CT core module
3757822015 Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3757823013 Noonan syndrome-like disorder with juvenile myelomonocytic leukemia en Synonym Active Entire term case sensitive SNOMED CT core module
3757824019 CBL (Cbl proto-oncogene) 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
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Finding site Face structure true Inferred relationship Existential restriction modifier 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia Is a Hereditary cancer-predisposing syndrome true Inferred relationship Existential restriction modifier
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia 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