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722037004: Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (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
3330287017 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330288010 MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330289019 MEHMO syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643127019 Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643128012 Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643161017 X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402789010 A rare X-linked syndromic intellectual disability characterized by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402790018 A rare X-linked syndromic intellectual disability characterised by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330286014 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330286014 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330287017 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330287017 Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330288010 MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330289019 MEHMO syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643127019 Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643128012 Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643161017 X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330290011 MEHMO syndrome has characteristics of severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity. Growth delay and diabetes are also present. To date, it has been described in seven boys, all of who died within the first two years of life. The causative gene has been located to the 21.1-22.13p region of the X chromosome and the syndrome appears to result from mitochondrial dysfunction. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402789010 A rare X-linked syndromic intellectual disability characterized by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402790018 A rare X-linked syndromic intellectual disability characterised by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3448881001000115 MEHMO-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6386691000241116 syndrome de MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6386701000241116 syndrome de déficience intellectuelle liée à l'X, crises d'épilepsie, hypogonadisme et hypogénitalisme, microcéphalie et obésité fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6386711000241119 syndrome de déficience intellectuelle, crises d'épilepsie, hypogonadisme et hypogénitalisme, microcéphalie et obésité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6386691000241116 syndrome de MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6386701000241116 syndrome de déficience intellectuelle liée à l'X, crises d'épilepsie, hypogonadisme et hypogénitalisme, microcéphalie et obésité fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6386711000241119 syndrome de déficience intellectuelle, crises d'épilepsie, hypogonadisme et hypogénitalisme, microcéphalie et obésité fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3448881001000115 MEHMO-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
MEHMO syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Is a retard mental false Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Is a Mitochondrial cytopathy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Is a Obesity true Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Has definitional manifestation Obese false Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
MEHMO syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
MEHMO syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Interprets Measured body weight (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
MEHMO syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
MEHMO syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
MEHMO syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
MEHMO syndrome Has interpretation Above reference range true Inferred relationship Existential restriction modifier (core metadata concept) 2
MEHMO syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept)
MEHMO syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3
MEHMO syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
MEHMO syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 4
MEHMO syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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