237612000: Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)

\Viscus structure finding (finding)\Abdominal organ finding\...

\Finding of pancreas\Disease of pancreas\Disorder of endocrine pancreas (disorder)\Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction

\Kidney finding\Kidney disease\...

\Hereditary nephropathy (disorder)\Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction

\Metabolic renal disease\Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction

\Head finding (finding)\Finding of brain\Disorder of brain\Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain\Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction

Descriptions:

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Multisystem disorder O-P	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Disorder of endocrine pancreas (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Finding site	Endocrine pancreatic structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	trouble multisytémique	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Disorder of endocrine system (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Disorder of body cavity (disorder)	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Disease of abdomen	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Abdominal organ finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Digestive system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Hereditary disorder of nervous system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Eighth cranial nerve finding	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Hereditary nephropathy (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	An absence seizure associated with eyelid myoclonia (myoclonic jerks of the eyelids and upward deviation of the eyes) often precipitated by closing the eyes or by light.	false	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Auditory system hereditary disorder	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Diabetes mellitus associated with genetic syndrome	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Neural hearing loss	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Finding site	Kidney structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Finding site	The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.	true	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Finding site	Vestibulocochlear nerve structure	true	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Finding site	Structure of auditory system (body structure)	true	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Interprets	Hearing	true	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Associated with	Genetic disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)	7
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Hereditary disorder of endocrine system (disorder)	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Central nervous system complication	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Disorder of brain	true	Inferred relationship	Existential restriction modifier (core metadata concept)
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	Is a	Metabolic renal disease	true	Inferred relationship	Existential restriction modifier (core metadata concept)

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
356099014	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
356100018	Herrmann syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
626366011	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
356099014	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
356099014	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
356100018	Herrmann syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
626366011	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
626366011	Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
161231000077115	myoclonie photo-induite, diabète sucré, surdité, néphropathie et dysfonctionnement cérébral	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
161231000077115	myoclonie photo-induite, diabète sucré, surdité, néphropathie et dysfonctionnement cérébral	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module