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778070003: Autosomal dominant primary microcephaly (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3737629019 Autosomal dominant primary microcephaly en Synonym Active Entire term case insensitive SNOMED CT core module
3737630012 Autosomal dominant primary microcephaly (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant primary microcephaly Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant primary microcephaly Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 1
Autosomal dominant primary microcephaly Is a Microcephalus false Inferred relationship Existential restriction modifier
Autosomal dominant primary microcephaly Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Autosomal dominant primary microcephaly Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Autosomal dominant primary microcephaly Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Autosomal dominant primary microcephaly Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier
Autosomal dominant primary microcephaly Finding site Brain structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant primary microcephaly Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant primary microcephaly Is a Congenital microcephaly true Inferred relationship Existential restriction modifier
Autosomal dominant primary microcephaly Finding site Head structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant primary microcephaly Has interpretation Below reference range true Inferred relationship Existential restriction modifier 2
Autosomal dominant primary microcephaly Interprets Birth head circumference true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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