The MalaCard for "narp" has been retired.
Searching MalaCards for entries containing "narp"
Searching MalaCards for entries containing "narp"
22 hits were found for 'narp'
| # | F | MCID | Name | MIFTS | Score |
|---|---|---|---|---|---|
| 1 | NRP003 | Neuropathy Ataxia Retinitis Pigmentosa Syndrome | 16.1 | 5.739 | |
| 2 | MTC015 | Mitochondrial Dna-associated Leigh Syndrome and Narp | 23.8 | 5.553 | |
| 3 | NRN002 | Neuronitis | 82.8 | 0.139 | |
| 4 | P | LGH001 | Leigh Disease | 51.3 | 0.113 |
| 5 | P | NRC002 | Narcolepsy | 71.7 | 0.113 |
| 6 | ADS002 | Adie Syndrome | 29.8 | 0.080 | |
| 7 | AMN003 | Amnestic Disorder | 25.2 | 0.080 | |
| 8 | ATX004 | Ataxia | 73.2 | 0.080 | |
| 9 | LGH002 | Leigh Syndrome Due to Cytochrome C Oxidase Deficiency | 9.7 | 0.080 | |
| 10 | LGH003 | Leigh Syndrome, French Canadian Type | 14.8 | 0.080 | |
| 11 | c | LGH005 | Leigh Syndrome (mtdna Deletion) | 5.7 | 0.080 |
| 12 | c | LGH006 | Leigh Syndrome (mtdna Mutation) | 2.0 | 0.080 |
| 13 | c | LGH007 | Leigh Syndrome (nuclear Dna Mutation) | 3.6 | 0.080 |
| 14 | LGH009 | Leigh Syndrome Due to Mitochondrial Complex I Deficiency | 20.4 | 0.080 | |
| 15 | LGH010 | Leigh Syndrome, Due to Cox Deficiency | 9.5 | 0.080 | |
| 16 | MHR001 | Mohr-tranebjaerg Syndrome | 32.6 | 0.080 | |
| 17 | PRN023 | Prion Disease | 78.3 | 0.080 | |
| 18 | P | RTN008 | Retinitis Pigmentosa | 71.6 | 0.080 |
| 19 | RTN023 | Retinitis | 82.5 | 0.080 | |
| 20 | SBC012 | Subcorneal Pustular Dermatosis | 38.3 | 0.080 | |
| 21 | SZR002 | Seizures | 70.7 | 0.080 | |
| 22 | XLN036 | X-linked Leigh Syndrome | 11.7 | 0.080 |