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1172593006: Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder)


Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4634518013 Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4634519017 Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome en Synonym Active Case insensitive SNOMED CT core
4634521010 A rare severe early-onset neurodegenerative encephalopathy with main characteristic developmental delay/regression, epilepsy, cortical atrophy, secondary hypomyelination and thin corpus callosum. Additional features include secondary microcephaly, hypotonia, spasticity, optic atrophy and skeletal anomalies. This syndrome is caused by biallelic pathogenic variants in TBCD gene (17q25.3), encoding tubulin folding co-factor D (TBCD), one of five co-chaperones required for microtubule assembly dynamics. The pattern of inheritance is autosomal recessive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Optic nerve finding true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Developmental delay true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Hereditary optic atrophy true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Cerebral atrophy true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Epilepsy true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Pathological process Pathological developmental process true Inferred relationship Some 3
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Finding site Structure of cerebrum true Inferred relationship Some 1
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Finding site Optic nerve structure true Inferred relationship Some 2
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Associated morphology Primary atrophy true Inferred relationship Some 2
Early-onset progressive diffuse brain atrophy, microcephaly, muscle weakness, optic atrophy syndrome Associated morphology Diffuse atrophy true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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