|
von recklinghausen disease
|
D009456 |
|
|
von recklinghausens disease
|
D009456 |
|
|
lipoprotein deficiency disease, HDL, familial
|
D052456 |
|
|
alpha-Lipoprotein deficiency disease, familial
|
D052456 |
|
|
sinus node disease, familial, autosomal recessive
|
24562 |
|
|
CPT1C autosomal dominant pure spastic paraplegia
|
14568 |
|
|
obsolete bile duct mucinous cystic neoplasm
|
3456.0 |
|
|
neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome
|
14562 |
|
|
megaloblastic anemia due to dihydrofolate reductase deficiency
|
13456 |
|
|
anterior segment dysgenesis 2
|
12456 |
|
|
anterior segment dysgenesis 2; ASGD2
|
http://purl.obolibrary.org/obo/MONDO_0012456 |
|
|
anterior segment dysgenesis 3
|
24456 |
|
|
anterior segment dysgenesis 3; ASGD3
|
http://purl.obolibrary.org/obo/MONDO_0024456 |
|
|
NECTIN4 ectodermal dysplasia-syndactyly syndrome
|
24565 |
|
|
primary thymic epithelial neoplasm
|
6456 |
|
