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13331008: Atrophy (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
22797016 Atrophy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
22798014 Atrophy, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
22799018 Simple atrophy en Synonym (core metadata concept) Inactive Entire term case insensitive (core metadata concept) SNOMED CT core
737978016 Atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1220945019 Atrophic en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1083641000241115 atrophie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

41 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Atrophy Is a Degenerative abnormality false Inferred relationship Some
Atrophy Is a dégénérescence false Inferred relationship Some
Atrophy Is a Degenerative abnormality true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Chorioretinal atrophy Associated morphology True Atrophy Inferred relationship Some 3
Gyrate atrophy Associated morphology True Atrophy Inferred relationship Some 2
Pigmented paravenous retinochoroidal atrophy (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Pigmented paravenous retinochoroidal atrophy (disorder) Associated morphology True Atrophy Inferred relationship Some 3
Keratosis follicularis, dwarfism, cerebral atrophy syndrome Associated morphology False Atrophy Inferred relationship Some 6
Helicoid peripapillary chorioretinal degeneration (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Helicoid peripapillary chorioretinal degeneration (disorder) Associated morphology True Atrophy Inferred relationship Some 3
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Charcot-Marie-Tooth disease type 2B1 (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) Associated morphology False Atrophy Inferred relationship Some 5
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) Associated morphology False Atrophy Inferred relationship Some 7
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) Associated morphology False Atrophy Inferred relationship Some 5
Neuralgic amyotrophy of left brachial plexus (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Neuralgic amyotrophy of left brachial plexus (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Neuralgic amyotrophy of right brachial plexus (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Neuralgic amyotrophy of right brachial plexus (disorder) Associated morphology False Atrophy Inferred relationship Some 3
Congenital onychoatrophy (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Atrophy of ear (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2U (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of left kidney Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of right kidney Associated morphology True Atrophy Inferred relationship Some 1
Senile involution of ovary (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Senile involution of ovary (disorder) Associated morphology False Atrophy Inferred relationship Some 1
Acquired atrophy of uterus Associated morphology True Atrophy Inferred relationship Some 1
Senile involution of ovary Associated morphology False Atrophy Inferred relationship Some 1
Acquired atrophy of ovary and fallopian tube Associated morphology True Atrophy Inferred relationship Some 2
Acquired atrophy of ovary and fallopian tube Associated morphology True Atrophy Inferred relationship Some 1
Acquired atrophy of fallopian tube Associated morphology True Atrophy Inferred relationship Some 1
Acquired cerebral atrophy (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) Associated morphology True Atrophy Inferred relationship Some 3
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Combined immunodeficiency with faciooculoskeletal anomalies syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Associated morphology True Atrophy Inferred relationship Some 2
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Associated morphology False Atrophy Inferred relationship Some 3
Autosomal dominant neovascular inflammatory vitreoretinopathy (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Charcot-Marie-Tooth disease type 2B5 Associated morphology True Atrophy Inferred relationship Some 1
Lattice degeneration of right retina (disorder) Associated morphology False Atrophy Inferred relationship Some 1
Lattice degeneration of left retina (disorder) Associated morphology False Atrophy Inferred relationship Some 1
Lattice degeneration of bilateral retinas (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Lattice degeneration of bilateral retinas (disorder) Associated morphology False Atrophy Inferred relationship Some 1
Optic atrophy of left eye Associated morphology True Atrophy Inferred relationship Some 1
Optic atrophy of right eye Associated morphology True Atrophy Inferred relationship Some 1
Optic atrophy of bilateral eyes (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Optic atrophy of bilateral eyes (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Severe X-linked intellectual disability Gustavson type (disorder) Associated morphology True Atrophy Inferred relationship Some 3
Keratosis follicularis, dwarfism, cerebral atrophy syndrome Associated morphology True Atrophy Inferred relationship Some 1
Intellectual disability, developmental delay, contracture syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Choroidal atrophy and alopecia syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Autosomal dominant Charcot-Marie-Tooth disease type 2Q Associated morphology True Atrophy Inferred relationship Some 1
Syphilitic optic atrophy Associated morphology True Atrophy Inferred relationship Some 1
Charcot-Marie-Tooth disease type 2R Associated morphology True Atrophy Inferred relationship Some 1
Bilateral atrophy of muscle of lower legs Associated morphology True Atrophy Inferred relationship Some 2
Bilateral atrophy of muscle of lower legs Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of left lower leg (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of right hand (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of left thigh Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of left shoulder Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of right lower leg (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of left upper arm (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of right thigh Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of right shoulder (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of left hand (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of muscle of right upper arm (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome (disorder) Associated morphology True Atrophy Inferred relationship Some 3
Autosomal recessive cerebral atrophy Associated morphology True Atrophy Inferred relationship Some 1
Congenital onychoatrophy (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons Associated morphology True Atrophy Inferred relationship Some 1
Autosomal dominant Charcot-Marie-Tooth disease type 2O Associated morphology True Atrophy Inferred relationship Some 1
Post-atrophic hyperplasia (morphologic abnormality) Is a True Atrophy Inferred relationship Some
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome Associated morphology True Atrophy Inferred relationship Some 1
Paving stone retinal degeneration of right eye (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Bilateral paving stone retinal degeneration Associated morphology False Atrophy Inferred relationship Some 3
Paving stone retinal degeneration of left eye (disorder) Associated morphology False Atrophy Inferred relationship Some 2
Follicular atrophoderma and basal cell epitheliomata Associated morphology True Atrophy Inferred relationship Some 2
Atrophy of iris of right eye Associated morphology True Atrophy Inferred relationship Some 1
Atrophy of iris of left eye (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Partial optic atrophy of right eye (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Bilateral partial optic atrophy Associated morphology True Atrophy Inferred relationship Some 1
Bilateral partial optic atrophy Associated morphology True Atrophy Inferred relationship Some 2
Partial optic atrophy of left eye Associated morphology True Atrophy Inferred relationship Some 1
Ataxia with tapetoretinal degeneration syndrome Associated morphology True Atrophy Inferred relationship Some 1
Lethal congenital contracture syndrome type 2 (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Vitreoretinal tuft of right eye Associated morphology True Atrophy Inferred relationship Some 1
Charcot-Marie-Tooth disease type 2P (disorder) Associated morphology True Atrophy Inferred relationship Some 1
Vitreoretinal tuft of left eye Associated morphology True Atrophy Inferred relationship Some 1
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome Associated morphology True Atrophy Inferred relationship Some 1
Vitreoretinal tuft of right eye Associated morphology True Atrophy Inferred relationship Some 3
Vitreoretinal tuft of left eye Associated morphology True Atrophy Inferred relationship Some 3
Retina - peripheral cystic tufts (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Peripheral retina - white without pressure Associated morphology True Atrophy Inferred relationship Some 2
Peripheral retina - white with pressure Associated morphology True Atrophy Inferred relationship Some 2
Vitreoretinal degeneration Associated morphology True Atrophy Inferred relationship Some 2
Zonular traction peripheral retinal tuft (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Vitreoretinal tuft (disorder) Associated morphology True Atrophy Inferred relationship Some 2
Noncystic peripheral retinal tuft (disorder) Associated morphology True Atrophy Inferred relationship Some 2

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