From: Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)
CHED1
CHED2
PPCD1
PPCD2
PPCD3
FECD1
FECD2
Inheritance
Dominant
Recessive
Sporadic or Dominant and more severe in females
Gene
20p11.2-q11.2 [3]
SLC4A11[4]
VSX1[5]
COL8A2[6]
TCF8[7]
13pTel-13q12.13 and 18q21.2-q21.32 [8, 9]
Onset
Early
Birth
Late, 4th decade