|
amelogenesis imperfecta, type IF
|
14560 |
|
|
amelogenesis imperfecta, type IF; AI1F
|
http://purl.obolibrary.org/obo/MONDO_0014560 |
|
|
macular dystrophy, vitelliform, 3; VMD3
|
http://purl.obolibrary.org/obo/MONDO_0024561 |
|
|
episodic muscle weakness, x-linked
|
C564565 |
|
|
pulmonic stenosis with Cafe-au-Lait spots
|
D009456 |
|
|
lissencephaly, x-linked, with ambiguous genitalia
|
C564563 |
|
|
3-methylglutaconic aciduria type VII
|
14561 |
|
|
pulmonic stenosis with cafe au lait spots
|
D009456 |
|
|
neonatal encephalopathy with non-epileptic myoclonus
|
100456 |
|
|
cerebroretinal microangiopathy with calcifications and cysts 1
|
24564 |
|
|
cerebroretinal microangiopathy with calcifications and cysts 1; CRMCC1
|
http://purl.obolibrary.org/obo/MONDO_0024564 |
|
|
3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
|
14561 |
|
|
3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia
|
14561 |
|
|
3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia; MEGCANN
|
http://purl.obolibrary.org/obo/MONDO_0014561 |
|
|
mental retardation, x-linked 58
|
C564566 |
|
