773627004: Porencephaly, microcephaly, bilateral congenital cataract syndrome (disorder)

\Neurological lesion\Lesion of brain\Congenital porencephaly\Porencephaly, microcephaly, bilateral congenital cataract syndrome

\Finding of brain\Disorder of brain\...

\Lesion of brain\Congenital porencephaly\Porencephaly, microcephaly, bilateral congenital cataract syndrome

\Congenital anomaly of brain\Congenital porencephaly\Porencephaly, microcephaly, bilateral congenital cataract syndrome

Descriptions:

Id Description Lang Type Status Case? Module

3724874010 Porencephaly, microcephaly, bilateral congenital cataract syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3724875011 Porencephaly, microcephaly, bilateral congenital cataract syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Hereditary disorder of the visual system	true	Inferred relationship	Existential restriction modifier
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Finding site	Brain structure	false	Inferred relationship	Existential restriction modifier	3
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Associated morphology	Congenital cavitation	false	Inferred relationship	Existential restriction modifier	3
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Finding site	Structure of lens of left eye	false	Inferred relationship	Existential restriction modifier	2
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Hereditary disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	3
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Congenital cataract of bilateral eyes	true	Inferred relationship	Existential restriction modifier
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Finding site	Structure of lens of right eye	false	Inferred relationship	Existential restriction modifier	1
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Congenital porencephaly	true	Inferred relationship	Existential restriction modifier
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Multiple system malformation syndrome	true	Inferred relationship	Existential restriction modifier
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Associated morphology	Cataract	false	Inferred relationship	Existential restriction modifier	1
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Associated morphology	Cataract	false	Inferred relationship	Existential restriction modifier	2
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Finding site	Structure of lens of left eye	true	Inferred relationship	Existential restriction modifier	3
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Associated morphology	Abnormally opaque structure	true	Inferred relationship	Existential restriction modifier	3
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Associated morphology	Cystic dilatation	true	Inferred relationship	Existential restriction modifier	1
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Associated morphology	Abnormally opaque structure	true	Inferred relationship	Existential restriction modifier	2
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Finding site	Brain structure	true	Inferred relationship	Existential restriction modifier	1
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Finding site	Structure of lens of right eye	true	Inferred relationship	Existential restriction modifier	2
Porencephaly, microcephaly, bilateral congenital cataract syndrome	Is a	Developmental hereditary disorder	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

Characteristic

Refinability

This concept is not in any reference sets

Id	Description	Lang	Type	Status	Case?	Module
3724874010	Porencephaly, microcephaly, bilateral congenital cataract syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3724875011	Porencephaly, microcephaly, bilateral congenital cataract syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module