|
dilated, 1BB cardiomyopathy
|
C567877 |
|
|
keratoconus with cataract
|
13678 |
|
|
growth retardation, cataract, hearing loss, and unusual appearance microcephaly
|
C567849 |
|
|
developmental delay, coarse facies, and early death growth retardation
|
C567856 |
|
|
Helicobacter pylori caused disease or disorder
|
6781 |
|
|
athabaskan severe combined immunodeficiency
|
C536786 |
|
|
xeroderma pigmentosum, complementation group c
|
C567886 |
|
|
spastic ataxia, charlevoix-saguenay type
|
C536787 |
|
|
autosomal recessive congenital 3 cataract
|
C567835 |
|
|
t-cell immunodeficiency, congenital alopecia, and nail dystrophy
|
C536781 |
|
|
type io congenital disorder of glycosylation
|
C567857 |
|
|
vitamin K deficiency bleeding in newborn
|
6784 |
|
|
Vitamin K deficiency bleeding in newborn
|
http://purl.obolibrary.org/obo/MONDO_0006784 |
|
|
homozygous 11P15-p14 deletion syndrome
|
11678 |
|
