Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandOptic Nerve Diseases (D009901)
..Starting node
..expandOptic Atrophy (D009896)

       Child Nodes:
........expandAl Gazali Khidr Prem Chandran syndrome (C535616)
........expandAl Gazali Sabrinathan Nair syndrome (C535617)
........expandBehr syndrome (C537669)
........expandCAPOS syndrome (C535351)
........expandCosteff optic atrophy syndrome (C535311)
........expandJensen syndrome (C537568)
........expandMental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature (C563810)
........expandMohr-Tranebjaerg syndrome (C535808)
........expandOptic Atrophies, Hereditary (D015418) Child30
........expandOPTIC ATROPHY 2 (OMIM:311050)
........expandOptic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
........expandOptic atrophy, X-linked (C537125)
........expandPEHO syndrome (C536317)
........expandSilengo Lerone Pelizza syndrome (C537336)
........expandSpastic Ataxia (C564815)
........expandSpastic Paraplegia, Optic Atrophy, and Neuropathy (C563702)
........expandTreft Sanborn Carey syndrome (C536544)
........expandWarburg Sjo Fledelius syndrome (C536681)
........expandWolfram Syndrome 2 (C565733)
........expandX-linked mental retardation Gustavson type (C536759)



 Sister Nodes: 
..expandLow Tension Glaucoma (D057066)
..expandOptic Atrophy (D009896) Child50
..expandOptic Disk Drusen (D015594) Child2
..expandOptic Nerve Aplasia, Bilateral (C563493)
..expandOptic Nerve Hypoplasia and Abnormalities of the Central Nervous System (C565949)
..expandOptic Nerve Hypoplasia, Bilateral (C563492)
..expandOptic Nerve Injuries (D020221)
..expandOptic Nerve Neoplasms (D019574) Child1
..expandOptic Neuritis (D009902) Child1
..expandOptic Neuropathy, Ischemic (D018917) Child1
..expandPapilledema (D010211) Child1
..expandPseudopapilledema (C562401)
..expandRoifman-Chitayat Syndrome (C567641)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:8272
Name:Optic Atrophy
Definition:Atrophy of the optic disk which may be congenital or acquired. This condition indicates a deficiency in the number of nerve fibers which arise in the RETINA and converge to form the OPTIC DISK; OPTIC NERVE; OPTIC CHIASM; and optic tracts. GLAUCOMA; ISCHEMIA; inflammation, a chronic elevation of intracranial pressure, toxins, optic nerve compression, and inherited conditions (see OPTIC ATROPHIES, HEREDITARY) are relatively common causes of this condition.
Alternative IDs:
ParentIDs:MESH:D009901
TreeNumbers:C10.292.700.225 |C11.640.451
Synonyms:Atrophy, Optic
Slim Mappings:Eye disease|Nervous system disease
Reference: MedGen: D009896
MeSH: D009896
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants