|
high density lipoprotein deficiency, type 1
|
8783 |
|
|
organomegaly, endocrinopathy, m protein, and skin changes syndrome polyneuropathy
|
D016878 |
|
|
choroid malignant melanoma
|
3878 |
|
|
malignant choroid melanoma
|
3878 |
|
|
optic choroid melanoma (disease)
|
3878 |
|
|
ichthyosis hypogonadism mental retardation epilepsy syndrome
|
C535878 |
|
|
anemia, hypochromic microcytic, with defect 1N iron metabolism
|
http://purl.obolibrary.org/obo/MONDO_0008788 |
|
|
anemia, hypochromic microcytic, with defect in iron metabolism
|
8788 |
|
|
anemia, hypochromic microcytic, with iron overload 1
|
8787 |
|
|
anemia, hypochromic microcytic, with iron overload 1; AHMIO1
|
http://purl.obolibrary.org/obo/MONDO_0008787 |
|
|
anemia, hypochromic microcytic, with iron overload type 1
|
8787 |
|
|
uterine corpus mullerian adenosarcoma
|
2878 |
|
|
mecp2-related severe neonatal encephalopathy
|
C566878 |
|
