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1148757008: Microcephaly (finding)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4551751014 Microcephaly (finding) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4551752019 Microcephalus en Synonym Active Entire term case insensitive SNOMED CT core module
4551753012 Microcephaly en Synonym Active Entire term case insensitive SNOMED CT core module

114 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microcephaly Has interpretation Below reference range true Inferred relationship Existential restriction modifier 1
Microcephaly Interprets Head circumference true Inferred relationship Existential restriction modifier 1
Microcephaly Is a Finding of head circumference true Inferred relationship Existential restriction modifier
Microcephaly Finding site Head structure true Inferred relationship Existential restriction modifier 2
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital microcephaly Is a True Microcephaly Inferred relationship Existential restriction modifier
Family history of microcephaly Associated finding True Microcephaly Inferred relationship Existential restriction modifier 1
Secondary microcephaly Is a True Microcephaly Inferred relationship Existential restriction modifier
Fetal microcephaly Is a True Microcephaly Inferred relationship Existential restriction modifier
Deficiency of leukotriene C4 synthase Is a True Microcephaly Inferred relationship Existential restriction modifier
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly Is a True Microcephaly Inferred relationship Existential restriction modifier
Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Microcephaly, thin corpus callosum, intellectual disability syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Severe neonatal onset encephalopathy with microcephaly Is a True Microcephaly Inferred relationship Existential restriction modifier
Child head circumference < 0.4th centile Is a True Microcephaly Inferred relationship Existential restriction modifier
Child head circumference = 0.4th centile Is a True Microcephaly Inferred relationship Existential restriction modifier
Child head circumference 0.5th - 1.9th centile Is a True Microcephaly Inferred relationship Existential restriction modifier
Child head circumference equal to 2nd centile Is a True Microcephaly Inferred relationship Existential restriction modifier
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Microcephaly, congenital cataract, psoriasiform dermatitis syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Severe intellectual disability, progressive postnatal microcephaly, midline stereotypic hand movements syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
X-linked intellectual developmental disorder Christianson type Is a True Microcephaly Inferred relationship Existential restriction modifier
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Intrauterine growth restriction, congenital multiple café au lait macules, increased sister chromatid exchange syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract Is a True Microcephaly Inferred relationship Existential restriction modifier
Congenital ichthyosis, microcephalus, tetraplegia syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Sanjad Sakati syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Progressive cerebello-cerebral atrophy Is a True Microcephaly Inferred relationship Existential restriction modifier
Inosine triphosphate pyrophosphohydrolase-related lethal infantile neurological disorder with cataract and cardiac involvement Is a True Microcephaly Inferred relationship Existential restriction modifier
Phospholipase A2 activating protein-associated neurodevelopmental disorder Is a True Microcephaly Inferred relationship Existential restriction modifier
Spastic tetraplegia, thin corpus callosum, progressive postnatal microcephaly syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier
Pyrroline-5-carboxylate reductase 2 related microcephaly, progressive leukoencephalopathy Is a True Microcephaly Inferred relationship Existential restriction modifier
Fatty acyl-coenzyme A reductase 1 deficiency Is a True Microcephaly Inferred relationship Existential restriction modifier
Ubiquitin specific peptidase 18 deficiency Is a True Microcephaly Inferred relationship Existential restriction modifier
Menke Hennekam syndrome Is a True Microcephaly Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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