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| Deafness_IsolatedAndComplex v1.260 | MEPE | Chirag Patel Marked gene: MEPE as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.260 | MEPE | Chirag Patel Gene: mepe has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.245 | Chirag Patel Copied gene MEPE from panel Deafness_Isolated | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.245 | MEPE |
Chirag Patel gene: MEPE was added gene: MEPE was added to Deafness_IsolatedAndComplex. Sources: Expert Review Amber,Expert Review Mode of inheritance for gene: MEPE was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MEPE were set to 30287925 Phenotypes for gene: MEPE were set to Nonsyndromic genetic hearing loss, MONDO:0019497, MEPE-related; hereditary congenital facial paresis; otosclerosis |
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