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1197215004: Microform holoprosencephaly (disorder)


Status: current, Primitive. Date: 28-Feb 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4695462014 Holoprosencephaly minor form en Synonym Active Case insensitive SNOMED CT core
4695463016 HPE (holoprosencephaly) minor form en Synonym Active Case sensitive SNOMED CT core
4695464010 Microform holoprosencephaly en Synonym Active Case insensitive SNOMED CT core
4695465011 Holoprosencephaly-like en Synonym Active Case insensitive SNOMED CT core
4695466012 Microform holoprosencephaly (disorder) en Fully specified name Active Case insensitive SNOMED CT core
4695467015 A benign form of holoprosencephaly with characteristics of midline defects without the typical holoprosencephaly defect in brain cleavage and which can variably manifest with microcephaly, hypotelorism, midline cleft lip and/or flat nose, choanal stenosis, pyriform sinus stenosis, coloboma as well as a single median maxillary incisor. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Microform holoprosencephaly Is a Holoprosencephaly sequence true Inferred relationship Some
Microform holoprosencephaly Occurrence Congenital true Inferred relationship Some 1
Microform holoprosencephaly Finding site Structure of head true Inferred relationship Some 1
Microform holoprosencephaly Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Microform holoprosencephaly Pathological process Pathological developmental process true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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