|
bpes with duane retraction syndrome
|
C566222 |
|
|
hemorrhagic disorder due to an acquired coagulation factor defect
|
15662.0 |
|
|
rare coagulopathy due to an acquired coagulation factor defect
|
http://purl.obolibrary.org/obo/MONDO_0015662 |
|
|
antibody deficiency due to defect in CD19
|
C566275 |
|
|
brachmann-de lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay
|
C566206 |
|
|
alzheimer disease, early-onset, with cerebral amyloid angiopathy
|
C566299 |
|
|
hyperlipemia with familial hypercholesterolemic xanthomatosis
|
C566263 |
|
|
alzheimer disease, familial, 1
|
C566298 |
|
|
hereditary benign erythroreticulosis
|
C566285 |
|
|
bpes, type i, autosomal recessive
|
C566222 |
|
|
distinctive face, hydrocephaly, and skeletal abnormalities axenfeld-rieger anomaly with partially absent eye muscles
|
C566234 |
|
|
aryl hydrocarbon hydroxylase inducibility
|
C566250 |
|
