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719405005: Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3316235018 Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3316236017 Leukoencephalopathy with metaphyseal chondrodysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3789576010 Leucoencephalopathy with metaphyseal chondrodysplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402096016 A rare genetic neurological disorder characterized by the association of hypomyelinating leukodystrophy with spondylometaphyseal dysplasia. Patients present in infancy with absent or delayed ability to walk independently, slowly progressive motor deterioration, spasticity, ataxia, proximal weakness, and joint contractures. Additional manifestations include mild cognitive impairment, short stature, scoliosis, enlarged and deformed joints, dysarthria, nystagmus, visual defects, and mildly dysmorphic features, among others. Mode of inheritance is X-linked recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402097013 A rare genetic neurological disorder characterised by the association of hypomyelinating leucodystrophy with spondylometaphyseal dysplasia. Patients present in infancy with absent or delayed ability to walk independently, slowly progressive motor deterioration, spasticity, ataxia, proximal weakness, and joint contractures. Additional manifestations include mild cognitive impairment, short stature, scoliosis, enlarged and deformed joints, dysarthria, nystagmus, visual defects, and mildly dysmorphic features, among others. Mode of inheritance is X-linked recessive. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Leukoencephalopathy true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Metaphyseal chondrodysplasia true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a X-linked hereditary disease false Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Hereditary disorder of nervous system false Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Finding site Cerebral white matter structure true Inferred relationship Some 2
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 3
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Occurrence Congenital false Inferred relationship Some 3
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Finding site Bone structure false Inferred relationship Some 3
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Finding site Bone structure true Inferred relationship Some 1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Interprets Height / growth measure true Inferred relationship Some 3
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a X-linked recessive hereditary disease true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Is a Cerebral degeneration (disorder) true Inferred relationship Some
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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