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782771007: Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3755705014 Mitochondrial DNA depletion syndrome hepatocerebrorenal form en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3755706010 Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3755707018 Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3761537018 A rare genetic mitochondrial DNA depletion syndrome characterised by neonatal or early-infantile onset hepatopathy (manifesting with hepatomegaly, cholestasis, increased transaminases, coagulopathy, hypoalbuminaemia, ascites, and/or liver failure), associated with renal tubulopathy and progressive neurodegenerative manifestations, which include muscular atrophy, hyporeflexia, ataxia, sensory neuropathy, epilepsy, sensorineural hearing impairment, psychomotor regression, athetosis, nystagmus, and/or ophthalmoplegia. Patients typically present with recurrent vomiting, severe failure to thrive, feeding difficulties, and fasting hypoglycaemia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3761538011 A rare genetic mitochondrial DNA depletion syndrome characterized by neonatal or early-infantile onset hepatopathy (manifesting with hepatomegaly, cholestasis, increased transaminases, coagulopathy, hypoalbuminemia, ascites, and/or liver failure), associated with renal tubulopathy and progressive neurodegenerative manifestations, which include muscular atrophy, hyporeflexia, ataxia, sensory neuropathy, epilepsy, sensorineural hearing impairment, psychomotor regression, athetosis, nystagmus, and/or ophthalmoplegia. Patients typically present with recurrent vomiting, severe failure to thrive, feeding difficulties, and fasting hypoglycemia. 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
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Digestive system hereditary disorder (disorder) true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Disorder of brain (disorder) true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Depletion of mitochondrial DNA true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Occurrence Congenital true Inferred relationship Some 3
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Renal tubular disorder true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Hereditary disorder of nervous system false Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Metabolic and genetic disorder affecting the liver true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Occurrence Congenital true Inferred relationship Some 1
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Hereditary nephropathy (disorder) true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Occurrence Congenital true Inferred relationship Some 2
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Finding site Cerebrum true Inferred relationship Some 3
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Finding site Liver structure true Inferred relationship Some 1
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Finding site Renal tubule structure (body structure) true Inferred relationship Some 2
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Metabolic renal disease true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Inherited metabolic disorder of nervous system true Inferred relationship Some
Mitochondrial DNA depletion syndrome hepatocerebrorenal form Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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