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

54036001: Oto-palato-digital syndrome, type I (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
89817016 Oto-palato-digital syndrome, type I en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
89818014 Taybi syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
792223014 Oto-palato-digital syndrome, type I (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330758019 The mildest form of otopalatodigital syndrome spectrum disorder, characterized by a generalized skeletal dysplasia, mild intellectual disability, conductive hearing loss, and typical facial anomalies. Caused by gain of function mutations in the gene FLNA (Xq28) that encodes filamin A. Inherited in an X-linked dominant manner. Male-to-male transmission has not been reported. The chance of transmitting the mutation in each pregnancy is 50%; males inheriting the mutation will be affected while females who inherit the mutation have a broad range of phenotypic expression. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330772011 The mildest form of otopalatodigital syndrome spectrum disorder, characterised by a generalised skeletal dysplasia, mild intellectual disability, conductive hearing loss, and typical facial anomalies. Caused by gain of function mutations in the gene FLNA (Xq28) that encodes filamin A. Inherited in an X-linked dominant manner. Male-to-male transmission has not been reported. The chance of transmitting the mutation in each pregnancy is 50%; males inheriting the mutation will be affected while females who inherit the mutation have a broad range of phenotypic expression. 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
Oto-palato-digital syndrome, type I Is a Oto-palato-digital syndrome, type II false Inferred relationship Some
Oto-palato-digital syndrome, type I Associated morphology Dysplasia false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Finding site Musculoskeletal structure of limb false Inferred relationship Some
Oto-palato-digital syndrome, type I Occurrence Congenital false Inferred relationship Some
Oto-palato-digital syndrome, type I Finding site Skeletal system structure false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Associated morphology Developmental anomaly false Inferred relationship Some
Oto-palato-digital syndrome, type I Finding site Bone structure false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Associated morphology Congenital anomaly false Inferred relationship Some 3
Oto-palato-digital syndrome, type I Associated morphology Congenital dysplasia false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Finding site Limb structure false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Associated morphology Congenital malformation false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Finding site Bone structure false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Associated morphology Congenital malformation false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Finding site Limb structure false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Associated morphology Congenital dysplasia false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Occurrence Congenital true Inferred relationship Some 3
Oto-palato-digital syndrome, type I Finding site Bone structure false Inferred relationship Some 3
Oto-palato-digital syndrome, type I Occurrence Congenital true Inferred relationship Some 4
Oto-palato-digital syndrome, type I Associated morphology Developmental anomaly false Inferred relationship Some 4
Oto-palato-digital syndrome, type I Finding site Face structure true Inferred relationship Some 4
Oto-palato-digital syndrome, type I Occurrence Congenital true Inferred relationship Some 5
Oto-palato-digital syndrome, type I Associated morphology Congenital dysplasia false Inferred relationship Some 3
Oto-palato-digital syndrome, type I Associated morphology Developmental anomaly false Inferred relationship Some 5
Oto-palato-digital syndrome, type I Finding site Limb structure true Inferred relationship Some 5
Oto-palato-digital syndrome, type I Is a Multiple malformation syndrome with facial-limb defects as major feature false Inferred relationship Some
Oto-palato-digital syndrome, type I Is a X-linked hereditary disease false Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Osteodysplasia false Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Oto-palato-digital syndrome, type I Associated morphology Developmental failure of fusion (morphologic abnormality) false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Occurrence Congenital true Inferred relationship Some 1
Oto-palato-digital syndrome, type I Is a Otopalatodigital syndrome false Inferred relationship Some
Oto-palato-digital syndrome, type I Finding site Palatal structure false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Finding site Ear structure true Inferred relationship Some 1
Oto-palato-digital syndrome, type I Occurrence Congenital true Inferred relationship Some 2
Oto-palato-digital syndrome, type I Pathological process (attribute) Pathological developmental process false Inferred relationship Some 1
Oto-palato-digital syndrome, type I Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Oto-palato-digital syndrome, type I Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4
Oto-palato-digital syndrome, type I Pathological process (attribute) Pathological developmental process true Inferred relationship Some 5
Oto-palato-digital syndrome, type I Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oto-palato-digital syndrome, type I Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Oto-palato-digital syndrome, type I Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 5
Oto-palato-digital syndrome, type I Finding site Bone structure true Inferred relationship Some 2
Oto-palato-digital syndrome, type I Associated morphology Congenital dysplasia false Inferred relationship Some 2
Oto-palato-digital syndrome, type I Associated morphology Developmental failure of fusion (morphologic abnormality) true Inferred relationship Some 3
Oto-palato-digital syndrome, type I Finding site Palatal structure true Inferred relationship Some 3
Oto-palato-digital syndrome, type I Associated morphology Dysplasia true Inferred relationship Some 2
Oto-palato-digital syndrome, type I Is a Congenital anomaly of palate false Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Congenital anomaly of limb true Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Auditory system hereditary disorder true Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Otopalatodigital syndrome spectrum disorder true Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Disorder of ear false Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Congenital anomaly of face (disorder) true Inferred relationship Some
Oto-palato-digital syndrome, type I Interprets Hearing true Inferred relationship Some 6
Oto-palato-digital syndrome, type I Is a Conductive hearing loss true Inferred relationship Some
Oto-palato-digital syndrome, type I Is a Congenital hearing disorder true Inferred relationship Some
Oto-palato-digital syndrome, type I Has interpretation Impaired true Inferred relationship Some 6
Oto-palato-digital syndrome, type I Is a Cleft palate true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start