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724174003: Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder)


Status: current, Not 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
3431514010 Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431515011 Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403261018 A rare syndromic neurological disorder characterized by the association of Möbius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. There have been no further reports since 1996. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403262013 A rare syndromic neurological disorder characterised by the association of Möbius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. There have been no further reports since 1996. 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
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Is a Peripheral axonal neuropathy true Inferred relationship Some
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Is a Congenital facial nerve palsy true Inferred relationship Some
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Is a Congenital hypogonadotropic hypogonadism (disorder) true Inferred relationship Some
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Finding site Facial nerve structure true Inferred relationship Some 4
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 6
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Finding site Gonadal endocrine structure true Inferred relationship Some 6
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 7
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Finding site Structure of pars distalis of pituitary (body structure) true Inferred relationship Some 7
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Has interpretation Absent true Inferred relationship Some 5
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Interprets Gross movement of body and limbs true Inferred relationship Some 5
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Interprets Movement true Inferred relationship Some 3
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Finding site Axon structure true Inferred relationship Some 1
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Is a Gross movement of body and limbs - finding true Inferred relationship Some
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder) Is a Nerve palsy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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