FHIR © HL7.org | Server Home | FHIR Server FHIR Server 3.7.4-SNAPSHOT | FHIR Version n/a User: [n/a]

1003371001: Micromelic dwarfism Fryn type (disorder)

Descriptions:

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Micromelic dwarfism Fryn type	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Micromelic dwarfism Fryn type	Pathological process (attribute)	Pathological developmental process (qualifier value)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Micromelic dwarfism Fryn type	Is a	Micromelia (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Micromelic dwarfism Fryn type	Associated morphology	Congenital smallness	false	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Micromelic dwarfism Fryn type	Finding site	Entire limb	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Micromelic dwarfism Fryn type	Associated morphology	Abnormal smallness (morphologic abnormality)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
4168099016	Micromelic dwarfism Fryn type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4168100012	Micromelic dwarfism Fryn type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4168099016	Micromelic dwarfism Fryn type	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
4168100012	Micromelic dwarfism Fryn type (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core