38146002: Congenital hypoplasia (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

64768019 Congenital hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

64773013 Rudimentary structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

64774019 Incomplete development en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

64775018 Underdevelopment en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

771355019 Congenital hypoplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

61031000052117 kongenital hypoplasi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
kongenital hypoplasi	Is a	Hypoplasia	false	Inferred relationship	Some
kongenital hypoplasi	Is a	kongenital anomali	false	Inferred relationship	Some
kongenital hypoplasi	Is a	medfödd missbildning	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	11
Hypotrichosis with juvenile macular degeneration syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	7
Hypotrichosis and intellectual disability syndrome Lopes type (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	4
Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	5
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	4
Congenital ichthyosis with hypotrichosis syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	2
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	5
Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	9
Hereditary hypotrichosis with recurrent skin vesicles syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Temple Baraitser syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Temple Baraitser syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	4
Hemifacial microsomia	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Hemifacial microsomia with radial defect syndrome (disorder)	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	2
Stimmler syndrome	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Stabilization of hypoplastic thumb	Direct morphology	False	kongenital hypoplasi	Inferred relationship	Some	3
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome	Associated morphology	False	kongenital hypoplasi	Inferred relationship	Some	2

Start Previous Page 5 of 5

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)