FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

77817004: Neu-Laxova syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
129141014 Neu-Laxova syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
818689017 Neu-Laxova syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1234170016 NLS - Neu-Laxova syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3788772015 3-phosphoglycerate dehydrogenase deficiency neonatal form en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neu-Laxova syndrome Is a Multiple malformation syndrome with unusual brain and/or neuromuscular findings false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Is a Microcephalus false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Is a Congenital anomaly of brain false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Finding site Entire brain false Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Associated morphology Congenital smallness false Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 4
Neu-Laxova syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Finding site Brain structure false Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Is a Autosomal recessive ichthyosis true Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Is a 3-Phosphoglycerate dehydrogenase deficiency true Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 4
Neu-Laxova syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Finding site Entire skin true Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Neu-Laxova syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Neu-Laxova syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Neu-Laxova syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 5
Neu-Laxova syndrome Finding site Head structure true Inferred relationship Existential restriction modifier 2
Neu-Laxova syndrome Interprets Birth head circumference true Inferred relationship Existential restriction modifier 5
Neu-Laxova syndrome Is a Congenital microcephaly true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start