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13331008: Atrophy (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
22797016 Atrophy en Synonym Active Entire term case insensitive SNOMED CT core module
22798014 Atrophy, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
22799018 Simple atrophy en Synonym Inactive Entire term case insensitive SNOMED CT core module
737978016 Atrophy (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1220945019 Atrophic en Synonym Active Entire term case insensitive SNOMED CT core 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 Existential restriction modifier
Atrophy Is a Degeneration false Inferred relationship Existential restriction modifier
Atrophy Is a Degenerative abnormality true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Chorioretinal atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Gyrate atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Pigmented paravenous retinochoroidal atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Pigmented paravenous retinochoroidal atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Keratosis follicularis, dwarfism, cerebral atrophy syndrome Associated morphology False Atrophy Inferred relationship Existential restriction modifier 6
Helicoid peripapillary chorioretinal degeneration Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Helicoid peripapillary chorioretinal degeneration Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Charcot-Marie-Tooth disease type 2B1 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Associated morphology False Atrophy Inferred relationship Existential restriction modifier 5
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Associated morphology False Atrophy Inferred relationship Existential restriction modifier 7
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome Associated morphology False Atrophy Inferred relationship Existential restriction modifier 5
Neuralgic amyotrophy of left brachial plexus Associated morphology False Atrophy Inferred relationship Existential restriction modifier 2
Neuralgic amyotrophy of left brachial plexus Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Neuralgic amyotrophy of right brachial plexus Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Neuralgic amyotrophy of right brachial plexus Associated morphology False Atrophy Inferred relationship Existential restriction modifier 3
Congenital onychoatrophy Associated morphology False Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of ear Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2U Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of left kidney Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of right kidney Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Senile involution of ovary Associated morphology False Atrophy Inferred relationship Existential restriction modifier 2
Senile involution of ovary Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Acquired atrophy of uterus Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Senile involution of ovary Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Acquired atrophy of ovary and fallopian tube Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Acquired atrophy of ovary and fallopian tube Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Acquired atrophy of fallopian tube Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Acquired cerebral atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Combined immunodeficiency with faciooculoskeletal anomalies syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Associated morphology False Atrophy Inferred relationship Existential restriction modifier 3
Autosomal dominant neovascular inflammatory vitreoretinopathy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Charcot-Marie-Tooth disease type 2B5 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lattice degeneration of right retina Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Lattice degeneration of left retina Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Lattice degeneration of bilateral retinas Associated morphology False Atrophy Inferred relationship Existential restriction modifier 2
Lattice degeneration of bilateral retinas Associated morphology False Atrophy Inferred relationship Existential restriction modifier 1
Optic atrophy of left eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Optic atrophy of right eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Optic atrophy of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Optic atrophy of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Severe X-linked intellectual disability Gustavson type Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Keratosis follicularis, dwarfism, cerebral atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Intellectual disability, developmental delay, contracture syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Choroidal atrophy and alopecia syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
X-linked intellectual disability with dysmorphism and cerebral atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2Q Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Syphilitic optic atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease type 2R Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of bilateral lower legs Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of muscle of bilateral lower legs Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left lower leg Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of right hand Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left thigh Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left shoulder Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of right lower leg Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left upper arm Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of right thigh Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of right shoulder Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of left hand Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of muscle of right upper arm Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Microcornea, myopic chorioretinal atrophy, telecanthus syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebral atrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Congenital onychoatrophy Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2O Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Post-atrophic hyperplasia Is a True Atrophy Inferred relationship Existential restriction modifier
Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Paving stone retinal degeneration of right eye Associated morphology False Atrophy Inferred relationship Existential restriction modifier 2
Paving stone retinal degeneration of bilateral eyes Associated morphology False Atrophy Inferred relationship Existential restriction modifier 3
Paving stone retinal degeneration of left eye Associated morphology False Atrophy Inferred relationship Existential restriction modifier 2
Follicular atrophoderma and basal cell epitheliomata Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Atrophy of iris of right eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Atrophy of iris of left eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Partial optic atrophy of right eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Partial optic atrophy of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Partial optic atrophy of bilateral eyes Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Partial optic atrophy of left eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Ataxia with tapetoretinal degeneration syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Lethal congenital contracture syndrome type 2 Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Vitreoretinal tuft of right eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease type 2P Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Vitreoretinal tuft of left eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome Associated morphology True Atrophy Inferred relationship Existential restriction modifier 1
Vitreoretinal tuft of right eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Vitreoretinal tuft of left eye Associated morphology True Atrophy Inferred relationship Existential restriction modifier 3
Retina - peripheral cystic tufts Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Peripheral retina - white without pressure Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Peripheral retina - white with pressure Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Vitreoretinal degeneration Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Zonular traction peripheral retinal tuft Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Vitreoretinal tuft Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2
Noncystic peripheral retinal tuft Associated morphology True Atrophy Inferred relationship Existential restriction modifier 2

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