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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
91769016 Hypocellularity en Synonym Active Entire term 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
Hypotrichosis with juvenile macular degeneration syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Achondrogenesis, type IB Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of left ventricular inflow tract Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Congenital pontocerebellar hypoplasia type 10 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital pontocerebellar hypoplasia type 10 Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital muscular dystrophy with cerebellar involvement Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Severe achondrolasia with developmental delay and acanthosis nigricans Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 5
Thoracomelic dysplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Hypoplastic chondrodystrophy Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Familial adrenal hypoplasia with absent pituitary luteinizing hormone Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Undergrowth of whole hand Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Right hypoplastic heart syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Marie Unna syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis and hypoplastic teeth Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Asymmetric crying face association Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Diaphragmatic hernia, abnormal face and distal limb anomalies Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 5
Diaphragmatic hernia, abnormal face and distal limb anomalies Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 4
Septo-optic dysplasia sequence Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Short-limb skeletal dysplasia with severe combined immunodeficiency Associated morphology False Hypoplasia Inferred relationship Existential restriction modifier 2
Intellectual disability, aphasia, shuffling gait, adducted thumbs syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Deficient mural leaflet of left ventricular component of common atrioventricular valve Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of cranial sinus Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Congenital hypoplasia of annulus fibrosus of aorta Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 4
Primary congenital hypoplasia of bilateral lungs Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Primary congenital hypoplasia of bilateral lungs Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of optic nerve due to central nervous system malformation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Optic nerve hypoplasia due to endocrine deficiency Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of right coronoid process of mandible Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of left coronoid process of mandible Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of right condyloid process of mandible Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Hypoplasia of left condyloid process of mandible Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Oculo-auriculo-vertebral spectrum Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Secondary hypoplasia of bilateral lungs Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Secondary hypoplasia of bilateral lungs Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
X-linked complicated corpus callosum dysgenesis Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Bilateral coronoid hypoplasia of mandible Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Bilateral condylar hypoplasia of mandible Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Microcephalus, brain defect, spasticity, hypernatremia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Endosteal hyperostoses with cerebellar hypoplasia Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 6
Aase syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Acquired hypoplasia of left zygomatic bone Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Acquired hypoplasia of right zygomatic bone Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Acquired hypoplasia of bilateral zygomatic bones Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Acquired hypoplasia of bilateral zygomatic bones Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Short stature, brachydactyly, obesity, global developmental delay syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Special AT-rich sequence-binding protein 2-associated syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 4
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Lethal brain and heart developmental defects syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Isolated hypoplasia of fovea centralis Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Deafness, enamel hypoplasia, nail defect syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 6
Hypoplasia of hypothalamus Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital anomalies, enteropathy syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 2
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 4
Cerebellar-facial-dental syndrome Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 3
Hypotrichosis with keratosis pilaris and lentiginosis Associated morphology True Hypoplasia Inferred relationship Existential restriction modifier 1
Biventricular repair of hypoplastic left heart syndrome Direct morphology False Hypoplasia Inferred relationship Existential restriction modifier
Biventricular repair of hypoplastic left heart syndrome Direct morphology False Hypoplasia Inferred relationship Existential restriction modifier 1

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