FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

62192003: Diprosopus (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
103356013 Diprosopus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
103358014 Monocephalus diprosopus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
801337019 Diprosopus (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
934491000172116 diprosopie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429871001000114 Diprosopus de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


14 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Diprosopus Is a Monster false Inferred relationship Some
Diprosopus Finding site Fetal structure false Inferred relationship Some
Diprosopus Occurrence Fetal period false Inferred relationship Some
Diprosopus Occurrence Congenital false Inferred relationship Some
Diprosopus Associated morphology Congenital malformation false Inferred relationship Some
Diprosopus Occurrence Congenital true Inferred relationship Some 1
Diprosopus Associated morphology anomalie du développement false Inferred relationship Some 1
Diprosopus Finding site Fetal structure false Inferred relationship Some 1
Diprosopus Is a Congenital anomaly of face (disorder) true Inferred relationship Some
Diprosopus Associated morphology Double structure false Inferred relationship Some 2
Diprosopus Occurrence Congenital false Inferred relationship Some 2
Diprosopus Finding site Face structure false Inferred relationship Some 2
Diprosopus Finding site Face structure true Inferred relationship Some 1
Diprosopus Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Diprosopus Associated morphology Double structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Cephalodiprosopus Is a True Diprosopus Inferred relationship Some
Diprosopus tetrophthalmus Is a True Diprosopus Inferred relationship Some
Opodidymus Is a True Diprosopus Inferred relationship Some
Janiceps Is a True Diprosopus Inferred relationship Some
Congenital double lip Is a True Diprosopus Inferred relationship Some
A rare, major congenital malformation characterized by complete duplication of the nose resulting in two fully developed noses often associated with choanal atresia, causing respiratory distress and necessitating surgical repair. Is a True Diprosopus Inferred relationship Some
Eyebrow duplication-syndactyly syndrome is characterized by partial duplication of the eyebrows and syndactyly of the fingers and toes. It has been described in three patients (a brother and sister and an isolated case). Skin hyperelasticity, hypertrichosis and long eyelashes, and abnormal periorbital wrinkling were also reported in some of the patients. Transmission is autosomal recessive. Is a True Diprosopus Inferred relationship Some
Distichiasis Is a False Diprosopus Inferred relationship Some
Congenital distichiasis Is a True Diprosopus Inferred relationship Some

Reference Sets

Description inactivation indicator reference set

GB English

US English

Back to Start