FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

1260097007: Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Dec 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5159126016 PADDAS syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5159127013 SCA47 - spinocerebellar ataxia type 47 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5159128015 Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5159129011 Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5159130018 PUM1-associated developmental disability, ataxia, seizure syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5159140015 A rare genetic syndromic intellectual disability characterised by developmental delay, intellectual disability, ataxia, and more variably seizures and short stature. Behavioural abnormalities may also be observed, along with variable facial and other dysmorphic features (such as broad nasal bridge, hypertelorism, almond-shaped eyes, high-arched palate and anomalies of the fingers and toes). Brain imaging may reveal dilated ventricles, small corpus callosum or posterior fossa abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5159141016 A rare genetic syndromic intellectual disability characterized by developmental delay, intellectual disability, ataxia, and more variably seizures and short stature. Behavioral abnormalities may also be observed, along with variable facial and other dysmorphic features (such as broad nasal bridge, hypertelorism, almond-shaped eyes, high-arched palate and anomalies of the fingers and toes). Brain imaging may reveal dilated ventricles, small corpus callosum or posterior fossa abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Is a Intellectual disability true Inferred relationship Some
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Is a Spinocerebellar ataxia true Inferred relationship Some
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Is a Developmental delay true Inferred relationship Some
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Interprets Intellectual ability (observable entity) true Inferred relationship Some 3
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 3
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Interprets Adaptation behavior (observable entity) true Inferred relationship Some 4
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Has interpretation Impaired true Inferred relationship Some 4
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Finding site Cerebellar structure true Inferred relationship Some 1
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 1
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Finding site Spinal cord structure true Inferred relationship Some 2
Pumilio RNA binding family member 1-associated developmental disability, ataxia, seizure syndrome (disorder) Associated morphology Degenerative abnormality true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start