| Name |
|---|
FCMTE2 Genefamilial cortical myoclonic tremor with epilepsy 2 |
FCMTE1 Genefamilial cortical myoclonic tremor with epilepsy 1 |
MENOQ2 GeneMenopause, natural, age at, QTL2 |
MENOQ3 GeneMenopause, natural, age at, QTL3 |
MENOQ1 Genemenopause, natural, age at, QTL |
MENOQ4 GeneMenopause, natural, age at, QTL4 |
MENAQ3 GeneMenarche, age at, QTL3 |
MENAQ2 GeneMenarche, age at, QTL2 |
MENAQ1 GeneMenarche, age at, QTL |
MCOPCT1 Genecataract, congenital, with microphthalmia |
CTRCT37 GeneCataract, congenital cerulean type, 5 |
CTRCT34 GeneCataract, autosomal recessive congenital 3 |
CTRCT35 Genecataract, congenital nuclear, autosomal recessive |
CTAA1 Genecataract, anterior polar 1 |
CTAA2 Genecataract, anterior polar 2 |
CTPP5 GeneCataract, posterior polar, 5 |
CTRCT25 GeneCataract, central pouch-like, with sutural opacities |
CTRCT27 GeneCataract, congenital, nuclear progressive |
CTRCT28 GeneCataract 28 |
CTPL1 Genecataract, pulverulent (autosomal recessive, early-onset) |
CCA1 Genecataract, congenital, cerulean type, 1 |
CCT Genecataract, congenital, total |
CCV Genecataract, congenital, Volkmann type |
CTRCT29 GeneCataract 29, coralliform |
DFCTRPS GeneDeafness, cataract, retinitis pigmentosa, and sperm abnormalities |
CTPP GeneCataract, posterior polar |