Phenotypes for disease #07145 (MITCH (Mitchell syndrome), OMIM:618960)

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Owner     

Individual ID     
0000347734 Mitchell syndrome MITCH see paper; ..., 7y-diffuse desquamatory rash, gait instability, ptosis with photophobia, hearing loss, abdominal pain, diarrhea, nausea, dysuria Isolated (sporadic) 07y - - - Johan den Dunnen 00460007
0000347738 - MITCH see paper; ..., diffused erythroderma with whitish fine scales, hyperkeratosis plaques with brown coarse scales, pruritus; no alopecia; hearing loss; reduced visual acuity; ataxia; polyneuropathy; normal to impaired cognition; no gastrointestinal symptoms; no dysuria; normal white matter demyelination Isolated (sporadic) 07y - 06y - Johan den Dunnen 00460013
0000347740 - MITCH see paper; ..., erythema, hyperkeratosis with gray-to-brown scales, fissures, follicular papules, pruritus; no alopecia; hearing loss; allergic conjunctivitis; ataxia; polyneuropathy; normal to impaired cognition; seizures; no gastrointestinal symptoms; no dysuria Isolated (sporadic) 04y - 00y00m40d - Johan den Dunnen 00460014
0000347741 progressive sensorineural deafness MITCH see paper; ..., ,progressive sensorineural deafness visual abnormalities, skin ichthyosis; infantile age gait ataxia, progressive worsening, 10y-loss of walking Unknown 11y - - - Johan den Dunnen 00460015
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.