Aplasia/Hypoplasia of the macula
Symptom Information:
All diseases associated with this symptom:
Adult-onset foveomacular vitelliform dystrophy | (Orphanet:99000) |
Alport syndrome | (Orphanet:63) |
Aniridia | (Orphanet:77) |
Best vitelliform macular dystrophy | (Orphanet:1243) |
Coats disease | (Orphanet:190) |
EEM syndrome | (Orphanet:1897) |
Hypotrichosis with juvenile macular degeneration | (Orphanet:1573) |
Infantile neuronal ceroid lipofuscinosis | (Orphanet:79263) |
Isolated aniridia | (Orphanet:250923) |
Knobloch syndrome | (Orphanet:1571) |
Neuroectodermal melanolysosomal disease | (Orphanet:33445) |
Ocular albinism | (Orphanet:284804) |
Oculocutaneous albinism | (Orphanet:55) |
Oculocutaneous albinism type 1A | (Orphanet:79431) |
Oculocutaneous albinism type 1B | (Orphanet:79434) |
Oculocutaneous albinism type 4 | (Orphanet:79435) |
Sjögren-Larsson syndrome | (Orphanet:816) |
Syndactyly - telecanthus - anogenital and renal malformations | (Orphanet:140952) |
Vici syndrome | (Orphanet:1493) |
Von Hippel-Lindau disease | (Orphanet:892) |
X-linked recessive ocular albinism | (Orphanet:54) |