OMOP Concept 36716144
MEHMO syndrome
StandardConditionSNOMED722037004Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
2 source codes normalize to MEHMO syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C537451 | MEHMO syndrome | Non-standard |
| Nebraska Lexicon | 722037004 | X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome | Non-standard |
Synonyms
Alternative names recorded for MEHMO syndrome across source vocabularies.
- Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- Intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome (disorder)
- MEHMO (mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity) syndrome
- Mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
- síndrome de retardo mental, convulsiones epilépticas, hipogonadismo e hipogenitalismo, microcefalia y obesidad
- síndrome de retardo mental, convulsiones epilépticas, hipogonadismo e hipogenitalismo, microcefalia y obesidad (trastorno)
- X-linked intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, obesity syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(30)Roll up to these when you need a wider cohort.
- 1Developmental hereditary disorder
- 1Intellectual disability
- 1Mitochondrial cytopathy
- 1Multiple system malformation syndrome
- 1Obesity
- 1X-linked recessive hereditary disease
- 2Behavior finding
- 2Congenital malformation syndrome
- 2Developmental disorder
- 2Disease
- 2Hereditary disease
- 2Impaired cognition
- 2Intellectual ability - finding
- 2Metabolic disease
- 2Neurodevelopmental disorder
- 2Obese
- 2X-linked hereditary disease
- 3Clinical finding
- 3Cognitive function finding
- 3Congenital malformation
- 3Genetic disease
- 3High body weight
- 3Intelligence finding
- 3Mental state, behavior and/or psychosocial function finding
- 3Sex-linked hereditary disorder
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