719161008: Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Mental state, behavior and/or psychosocial function finding (finding)\Behavior finding\Intelligenzminderung\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Functional finding\Cognitive function finding (finding)\Impaired cognition (finding)\Intelligenzminderung\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Functional finding\Cognitive function finding (finding)\Intellectual ability - finding\Intelligenzminderung\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intelligenzminderung\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder (disorder)\X-linked hereditary disease\X-linked recessive hereditary disease\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Disease\Disorder of foetus and/or newborn\Congenital disease\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Disease\Developmental disorder (disorder)\Neurodevelopmental disorder\Intelligenzminderung\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Disease\Developmental disorder (disorder)\Developmental hereditary disorder\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)
• \Disease\Developmental disorder (disorder)\Congenital malformation\Congenital malformation syndrome\Multiple system malformation syndrome\Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (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
3315210015	Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315211016	Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315212011	Syndromic X-linked intellectual disability due to JARID1C mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315213018	Syndromic X-linked intellectual disability due to JARID1C (jumonji at-rich interactive domain 1c) mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5401980019	A rare multiple congenital anomalies/dysmorphic syndrome characterized by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech, and behavioral problems.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401981015	A rare multiple congenital anomalies/dysmorphic syndrome characterised by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech, and behavioural problems.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3315210015	Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315211016	Syndromic X-linked intellectual disability due to jumonji at-rich interactive domain 1c mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315212011	Syndromic X-linked intellectual disability due to JARID1C mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315213018	Syndromic X-linked intellectual disability due to JARID1C (jumonji at-rich interactive domain 1c) mutation	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
3315214012	This syndrome is characterised by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech and behavioural problems. To date, it has been described in less than 15 families. Transmission is X-linked recessive and the syndrome is caused by mutations in the JARID1C (SMCX) gene encoding a JmjC-domain protein with histone demethylase activity.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3315215013	This syndrome is characterized by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech and behavioral problems. To date, it has been described in less than 15 families. Transmission is X-linked recessive and the syndrome is caused by mutations in the JARID1C (SMCX) gene encoding a JmjC-domain protein with histone demethylase activity.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401980019	A rare multiple congenital anomalies/dysmorphic syndrome characterized by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech, and behavioral problems.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5401981015	A rare multiple congenital anomalies/dysmorphic syndrome characterised by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech, and behavioural problems.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3415801001000112	Intelligenzminderung, X-chromosomale, syndromale, Typ Claes-Jensen	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
3415801001000112	Intelligenzminderung, X-chromosomale, syndromale, Typ Claes-Jensen	de	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Reference Sets

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

Back to Start