FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

93249003: Congenital hypoplasia of cerebrum (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
154287010 Congenital hypoplasia of cerebrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154288017 Congenital small cerebrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836942016 Congenital hypoplasia of cerebrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
154287010 Congenital hypoplasia of cerebrum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154287010 Congenital hypoplasia of cerebrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154288017 Congenital small cerebrum en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
154288017 Congenital small cerebrum en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
836942016 Congenital hypoplasia of cerebrum (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
836942016 Congenital hypoplasia of cerebrum (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4708671000241110 hypoplasie du cerebrum fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4708671000241110 hypoplasie du cerebrum fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital hypoplasia of cerebrum Is a Congenital hypoplasia of part of brain true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of cerebrum Is a dysgénésie cérébrale false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of cerebrum Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of cerebrum Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Associated morphology Congenital hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of cerebrum Associated morphology Hypoplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of cerebrum Finding site The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica. false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital hypoplasia of cerebrum Is a Anomalies of cerebrum false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of cerebrum Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital hypoplasia of cerebrum Is a Congenital anomaly of cerebrum (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Hypoplasia of corpus callosum Is a True Congenital hypoplasia of cerebrum Inferred relationship Existential restriction modifier (core metadata concept)
Short stature-pituitary and cerebellar defects-small sella turcica syndrome is characterized by short stature, anterior pituitary hormone deficiency, small sella turcica, and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of a large French kindred. Ectopia of the posterior hypophysis was observed in some patients. The syndrome is transmitted as a dominantly inherited trait and is caused by a germline mutation within the LIM-homeobox transcription factor LHX4 gene (1q25). Is a True Congenital hypoplasia of cerebrum Inferred relationship Existential restriction modifier (core metadata concept)
Isolated unilateral hemispheric cerebellar hypoplasia is a rare, non-syndromic cerebellar malformation characterized by loss of volume in the right or left cerebellar hemisphere, with intact vermis and no other neurological anomalies (i.e. normal cerebral hemispheres, fourth ventricle, pons, medulla and midbrain). Patients may be asymptomatic or may present developmental and speech delay, hypotonia, abnormal ocular movements, persistent headaches and/or peripheral vertigo and ataxia. Neurological examination is otherwise normal. Is a True Congenital hypoplasia of cerebrum Inferred relationship Existential restriction modifier (core metadata concept)
Isolated bilateral hemispheric cerebellar hypoplasia (disorder) Is a True Congenital hypoplasia of cerebrum Inferred relationship Existential restriction modifier (core metadata concept)
Septo-optic dysplasia sequence Is a True Congenital hypoplasia of cerebrum Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start