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718574003: syndroom van palatoschisis, coloboom en doofheid (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312811015 Abruzzo Erickson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312812010 CHARGE-like syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3312814011 Cleft palate with coloboma of eye and deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3312815012 Cleft palate with coloboma of eye and deafness syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6115381000146111 palatoschisis-coloboom-doofheid-syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6115391000146113 CHARGE-achtig syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6115411000146113 syndroom van Abruzzo-Erickson nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6115421000146115 gespleten gehemelte-coloboom-doofheid-syndroom nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6675191000146115 syndroom van palatoschisis, coloboom en doofheid (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6675201000146118 syndroom van palatoschisis, coloboom en doofheid nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3312813017 A multiple congenital anomalies syndrome with manifestations of cleft palate, ocular coloboma, hypospadias, mixed conductive-sensorineural hearing loss, short stature and radio-ulnar synostosis. To date, 4 cases have been described in the literature. These manifestations overlap with those of CHARGE syndrome, however, in contrast to CHARGE syndrome, patients with Abruzzo-Erikson syndrome do not show intellectual disability, choanal atresia or genital hypoplasia. Inherited in an X-linked recessive manner, with a carrier female having a 50% chance of transmitting the mutation to her offspring. 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
Abruzzo Erickson syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
Abruzzo Erickson syndrome Is a Cleft palate true Inferred relationship Some
Abruzzo Erickson syndrome Is a Congenital ocular coloboma (disorder) true Inferred relationship Some
Abruzzo Erickson syndrome Is a X-linked hereditary disease false Inferred relationship Some
Abruzzo Erickson syndrome Is a Hearing loss associated with syndrome true Inferred relationship Some
Abruzzo Erickson syndrome Is a Auditory system hereditary disorder false Inferred relationship Some
Abruzzo Erickson syndrome Is a Digestive system hereditary disorder (disorder) false Inferred relationship Some
Abruzzo Erickson syndrome Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Abruzzo Erickson syndrome Finding site Ear structure true Inferred relationship Some 3
Abruzzo Erickson syndrome Associated morphology Congenital failure of fusion false Inferred relationship Some 4
Abruzzo Erickson syndrome Occurrence Congenital false Inferred relationship Some 4
Abruzzo Erickson syndrome Finding site Palatal structure false Inferred relationship Some 4
Abruzzo Erickson syndrome Associated morphology Congenital failure of fusion false Inferred relationship Some 3
Abruzzo Erickson syndrome Occurrence Congenital true Inferred relationship Some 3
Abruzzo Erickson syndrome Finding site Eye structure false Inferred relationship Some 3
Abruzzo Erickson syndrome Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 1
Abruzzo Erickson syndrome Occurrence Congenital true Inferred relationship Some 1
Abruzzo Erickson syndrome Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 2
Abruzzo Erickson syndrome Occurrence Congenital true Inferred relationship Some 2
Abruzzo Erickson syndrome Finding site Palatal structure true Inferred relationship Some 1
Abruzzo Erickson syndrome Finding site Eye structure true Inferred relationship Some 2
Abruzzo Erickson syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Abruzzo Erickson syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Abruzzo Erickson syndrome Is a Congenital hearing disorder false Inferred relationship Some
Abruzzo Erickson syndrome Finding site Structure of auditory system (body structure) false Inferred relationship Some 3
Abruzzo Erickson syndrome Interprets Hearing true Inferred relationship Some 4
Abruzzo Erickson syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Abruzzo Erickson syndrome Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 5
Abruzzo Erickson syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 5
Abruzzo Erickson syndrome Occurrence Congenital false Inferred relationship Some 5
Abruzzo Erickson syndrome Finding site Bone structure of head false Inferred relationship Some 5
Abruzzo Erickson syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Abruzzo Erickson syndrome Is a X-linked recessive hereditary disease true Inferred relationship Some
Abruzzo Erickson syndrome Is a Congenital mixed conductive and sensorineural hearing loss true Inferred relationship Some
Abruzzo Erickson syndrome Has interpretation Impaired true Inferred relationship Some 4
Abruzzo Erickson syndrome Is a X-linked sensorineural hearing loss true Inferred relationship Some
Abruzzo Erickson syndrome Is a Congenital hearing loss (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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