FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.1  |  FHIR Version n/a  User: [n/a]

41086002: Congenital smallness (morphologic abnormality)


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

Descriptions:

Id Description Lang Type Status Case? Module
68540011 Congenital smallness en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
777834016 Congenital smallness (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital smallness Is a Congenital growth alteration false Inferred relationship Some
Congenital smallness Is a Growth alteration true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Reconstruction of microtia with flap (procedure) Direct morphology True Congenital smallness Inferred relationship Some 1
Microphthalmos of right eye Associated morphology True Congenital smallness Inferred relationship Some 1
Microphthalmos of left eye Associated morphology True Congenital smallness Inferred relationship Some 1
Reconstruction of microtia with graft (procedure) Direct morphology True Congenital smallness Inferred relationship Some 2
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome Associated morphology True Congenital smallness Inferred relationship Some 3
Occipital pachygyria and polymicrogyria (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome Associated morphology True Congenital smallness Inferred relationship Some 2
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome Associated morphology True Congenital smallness Inferred relationship Some 4
Reduction anomaly of hypothalamus Associated morphology False Congenital smallness Inferred relationship Some 1
Megacystis, microcolon, hypoperistalsis syndrome Associated morphology True Congenital smallness Inferred relationship Some 2
Seckel syndrome Associated morphology True Congenital smallness Inferred relationship Some 2
Diastrophic dysplasia Associated morphology True Congenital smallness Inferred relationship Some 2
Thrombocytopathy, asplenia and miosis (disorder) Associated morphology True Congenital smallness Inferred relationship Some 5
Neu-Laxova syndrome Associated morphology True Congenital smallness Inferred relationship Some 2
Barber-Say syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 3
Microphthalmos co-occurrent with congenital ocular coloboma of bilateral eyes (disorder) Associated morphology True Congenital smallness Inferred relationship Some 3
Microphthalmos co-occurrent with congenital ocular coloboma of bilateral eyes (disorder) Associated morphology True Congenital smallness Inferred relationship Some 4
Microcornea of bilateral eyes (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Microcornea of bilateral eyes (disorder) Associated morphology True Congenital smallness Inferred relationship Some 2
Bilateral microphthalmos Associated morphology True Congenital smallness Inferred relationship Some 1
Bilateral microphthalmos Associated morphology True Congenital smallness Inferred relationship Some 2
Common atrioventricular valve with unbalanced commitment of valve to right ventricle (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Bilateral frontal polymicrogyria Associated morphology True Congenital smallness Inferred relationship Some 1
Bilateral frontoparietal polymicrogyria (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Bilateral generalized polymicrogyria (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Bilateral parasagittal parieto-occipital polymicrogyria Associated morphology True Congenital smallness Inferred relationship Some 1
Bilateral frontoparietal polymicrogyria (disorder) Associated morphology True Congenital smallness Inferred relationship Some 2
Bilateral parasagittal parieto-occipital polymicrogyria Associated morphology True Congenital smallness Inferred relationship Some 2
Microcephaly with simplified gyral pattern Associated morphology True Congenital smallness Inferred relationship Some 1
Microphthalmos due to branchio-oculo-facial syndrome Associated morphology True Congenital smallness Inferred relationship Some 1
Microlissencephaly Associated morphology True Congenital smallness Inferred relationship Some 1
Microphthalmos due to Fryns syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Microphthalmos due to Delleman syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Micromelic dwarfism Fryn type Associated morphology True Congenital smallness Inferred relationship Some 1
Congenital microcephaly (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Stimmler syndrome Associated morphology True Congenital smallness Inferred relationship Some 1
Jawad syndrome Associated morphology True Congenital smallness Inferred relationship Some 1
Congenital microencephaly (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Telomere maintenance 2-related intellectual disability, neurodevelopmental disorder (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome Associated morphology True Congenital smallness Inferred relationship Some 1
Colobomatous macrophthalmia with microcornea syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 3
Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome Associated morphology True Congenital smallness Inferred relationship Some 1
Reconstruction of microtia with free flap and microvascular anastomosis Direct morphology True Congenital smallness Inferred relationship Some 3
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 2
Microcephalic osteodysplastic primordial dwarfism type II Associated morphology True Congenital smallness Inferred relationship Some 2
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Ring finger protein 13-related severe early-onset epileptic encephalopathy (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
19p13.3 microduplication syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 3
Autosomal dominant myopia, midfacial retrusion, sensorineural hearing loss, rhizomelic dysplasia syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 2
Isolated microspherophakia (disorder) Associated morphology True Congenital smallness Inferred relationship Some 2
Microphthalmia, microtia, fetal akinesia syndrome Associated morphology True Congenital smallness Inferred relationship Some 2
Microphthalmia, microtia, fetal akinesia syndrome Associated morphology True Congenital smallness Inferred relationship Some 3
Microphthalmia, microtia, fetal akinesia syndrome Associated morphology True Congenital smallness Inferred relationship Some 4
Syndromic nanophthalmos due to Kenny-Caffey syndrome Associated morphology True Congenital smallness Inferred relationship Some 1
DNA replication fork stabilization factor DONSON-related microcephaly, short stature, limb abnormalities spectrum (disorder) Associated morphology True Congenital smallness Inferred relationship Some 2
NDE1-related microhydranencephaly Associated morphology True Congenital smallness Inferred relationship Some 1
Cerebellar-facial-dental syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 4
Microcephaly, intellectual disability, sensorineural hearing loss, epilepsy, abnormal muscle tone syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1
Congenital cataract microcornea with corneal opacity Associated morphology True Congenital smallness Inferred relationship Some 2
Short rib polydactyly syndrome type 5 Associated morphology True Congenital smallness Inferred relationship Some 2
Microcephaly, facial dysmorphism, ocular anomalies, multiple congenital anomalies syndrome (disorder) Associated morphology True Congenital smallness Inferred relationship Some 1

Start Previous Page 4 of 4


This concept is not in any reference sets

Back to Start