FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

1230295000: B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Jun 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5068781011 B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068782016 BILU (B-cell immunodeficiency, limb, urogenital) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068783014 B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068784015 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterised by almost complete lack of B-cells and severe hypogammaglobulinaemia, anomalies of the hands and feet, urogenital malformations and characteristic facial dysmorphism (including microcephaly, highly arched eyebrows, hypoplastic alae nasi and micrognathia). Most patients are developmentally normal although moderate intellectual disability has also been described. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5068785019 A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by almost complete lack of B-cells and severe hypogammaglobulinemia, anomalies of the hands and feet, urogenital malformations and characteristic facial dysmorphism (including microcephaly, highly arched eyebrows, hypoplastic alae nasi and micrognathia). Most patients are developmentally normal although moderate intellectual disability has also been described. 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
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Is a Congenital agammaglobulinemia true Inferred relationship Some
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Some
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Is a Congenital abnormality of foot and toes (disorder) true Inferred relationship Some
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Is a Genitourinary congenital anomalies true Inferred relationship Some
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Is a Congenital anomaly of hand (disorder) true Inferred relationship Some
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Is a Genetic disease true Inferred relationship Some
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Finding site Structure of genitourinary system (body structure) true Inferred relationship Some 1
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Finding site Foot structure true Inferred relationship Some 2
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Finding site Hand structure true Inferred relationship Some 3
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Finding site Face structure true Inferred relationship Some 4
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Occurrence Congenital true Inferred relationship Some 5
B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome (disorder) Pathological process (attribute) Abnormal immune process (qualifier value) true Inferred relationship Some 5

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Description inactivation indicator reference set

Back to Start