| Disease Browser
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Parent Node:
 Dementia (D003704) | Parent Node:
Hearing Loss, Central (D006313) | Parent Node:
Optic Atrophy (D009896) | ..Starting node
.. Jensen syndrome (C537568)
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Child Nodes:
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Sister Nodes: | ..Al Gazali Khidr Prem Chandran syndrome (C535616)
| ..Al Gazali Sabrinathan Nair syndrome (C535617)
| ..Behr syndrome (C537669)
| ..CAPOS syndrome (C535351)
| ..Costeff optic atrophy syndrome (C535311)
| ..Jensen syndrome (C537568)
| ..Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature (C563810)
| ..Mohr-Tranebjaerg syndrome (C535808)
| ..Optic Atrophies, Hereditary (D015418)  30
| ..OPTIC ATROPHY 2 (OMIM:311050)
| ..Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Dominant (C563497)
| ..Optic atrophy, X-linked (C537125)
| ..PEHO syndrome (C536317)
| ..Silengo Lerone Pelizza syndrome (C537336)
| ..Spastic Ataxia (C564815)
| ..Spastic Paraplegia, Optic Atrophy, and Neuropathy (C563702)
| ..Treft Sanborn Carey syndrome (C536544)
| ..Warburg Sjo Fledelius syndrome (C536681)
| ..Wolfram Syndrome 2 (C565733)
| ..X-linked mental retardation Gustavson type (C536759)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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| Term ID: | 5960 |
| Name: | Jensen syndrome |
| Definition: | |
| Alternative IDs: | OMIM:311150 |
| ParentIDs: | MESH:D003704|MESH:D006313|MESH:D009896 |
| TreeNumbers: | C09.218.458.341.887.432/C537568 |C09.218.807.186.432/C537568 |C10.228.140.068.432/C537568 |C10.228.140.380/C537568 |C10.292.700.225/C537568 |C10.597.751.418.341.887.432/C537568 |C11.640.451/C537568 |C23.888.592.763.393.341.887.432/C537568 |F03.087.400/C537568 |
| Synonyms: | JENSEN SYNDROME |Nerve deafness optic nerve atrophy, and dementia |Opticoacoustic Nerve Atrophy With Dementia |Opticoacustic nerve atrophy with dementia |Syndrome of opticoacoustic nerve atrophy with dementia |
| Slim Mappings: | Ear-nose-throat disease|Eye disease|Mental disorder|Nervous system disease|Signs and symptoms |
| Reference: |
MedGen: C537568
MeSH: C537568
OMIM: 311150;
Genes: TIMM8A; | | Phenotypes | | | Disease Causing ClinVar Variants | |
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