|
erythrokeratodermia Figurata, congenital familial, 1N plaques
|
http://purl.obolibrary.org/obo/MONDO_0017851 |
|
|
keratoconus (disease) caused by mutation in VSX1
|
7851 |
|
|
erythrokeratodermia figurata, congenital familial, in plaques
|
17851 |
|
|
progressive symmetric erythrokeratodermia
|
17851 |
|
|
progressive symmetric erythrokeratodermia, Gottron type
|
17851 |
|
|
erythrokeratodermia Figurata variabilis
|
17851 |
|
|
posterior capsular rupture, ocular
|
D057851 |
|
|
erythrokeratodermia progressiva symmetrica
|
17851 |
|
|
keratoderma palmoplantaris transgrediens
|
17851 |
|
|
erythrokeratodermia variabilis with erythema gyratum repens
|
17851 |
|
