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55199003: Hypoplasia (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
91766011 Hypoplasia en Synonym Active Entire term case insensitive SNOMED CT core module
91767019 Hypoplasia, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
91768012 Acquired hypoplasia, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
91769016 Hypocellularity en Synonym Active Entire term case insensitive SNOMED CT core module
91770015 Acquired hypoplasia en Synonym Inactive Only initial character case insensitive SNOMED CT core module
793513011 Hypoplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypoplasia Is a Maturation defect true Inferred relationship Existential restriction modifier
Hypoplasia Is a Developmental anomaly false Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital hypoplasia of ulna and intellectual disability syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Brachymorphism with onychodysplasia and dysphalangism syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 4
Deafness, enamel hypoplasia, nail defect syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 9
Diaphragmatic defect, limb deficiency, skull defect syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 7
Limb mammary syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 4
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 5
Agnathia, holoprosencephaly, situs inversus syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 2
Distal limb deficiency with micrognathia syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 6
Thickened earlobe with conductive deafness syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 6
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 3
Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 6
Congenital pulmonary hypoplasia due to prolonged premature rupture of membranes Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital pulmonary hypoplasia due to lung space occupying lesion Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 2
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 4
Congenital hypoplasia of patella Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of right ventricular outflow tract and trabecular area Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 4
Isolated optic nerve hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 2
Splenogonadal fusion, limb defect, micrognathia syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 7
Congenital hypoplasia of ulna and split foot syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 5
Hypoplasia of mandibular condyle Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Familial adrenocortical hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Congenital hypoplasia of right optic nerve Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of left optic nerve Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of bilateral optic nerves Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of bilateral optic nerves Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Congenital hypoplasia of odontoid process of axis Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of sacrum Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Goldenhar syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of auditory canal Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of left kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of right kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Agenesis of left kidney co-occurrent with hypoplasia of right kidney Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 3
Agenesis of right kidney co-occurrent with hypoplasia of left kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Spondyloperipheral dysplasia with short ulna syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Porencephaly, cerebellar hypoplasia, internal malformations syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 2
Angio-osteohypotrophic syndrome Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 1
Ask-Upmark kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypertrophy of left kidney co-occurrent and due to congenital hypoplasia of right kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Angio-osteohypotrophic syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Hypertrophy of right kidney co-occurrent and due to congenital hypoplasia of left kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Isolated hypoplasia of cerebellar vermis Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Isolated unilateral hemispheric cerebellar hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Transient hypoplastic anemia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Congenital hypoplastic anemia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Double aortic arch with dominant left arch and hypoplasia of right arch Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Double aortic arch with dominant right arch and hypoplasia of left arch Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Acquired micrognathia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 1
Metaphyseal chondrodysplasia, McKusick type Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital hypoplasia of entire upper limb Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of part of upper limb Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Choanal atresia with radial ray hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
X-linked cerebral, cerebellar, coloboma syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Isolated bilateral hemispheric cerebellar hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Polymicrogyria with optic nerve hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Thumb deformity, alopecia, pigmentation anomaly syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Parietal foramina with clavicular hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital pontocerebellar hypoplasia type 4 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Agnathia, holoprosencephaly, situs inversus syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 3 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Bilateral renal hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 1 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital transverse mandibular hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 8 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital micrognathism Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Syndromic hypoplasia of orbital border Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Intellectual disability, truncal obesity, retinal dystrophy and micropenis syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of corpus callosum Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of right ventricular outflow tract and trabecular area Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of right ventricular inflow tract Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of right ventricular outflow tract Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital vertical mandibular hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Testicular regression syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 7 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital pulmonary hypoplasia due to prolonged premature rupture of membranes Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Intrahepatic biliary hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pulmonary hypoplasia due to lung space occupying lesion Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Septo-optic dysplasia sequence Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Fibulo-ulnar hypoplasia and renal anomalies syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of ulna and split foot syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Pulmonary hypoplasia associated with short gestation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Oligomeganephronic hypoplasia of kidney Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Cerebro-costo-mandibular syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 2 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of cardiac ventricle Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 6 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital horizontal mandibular hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1

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