All terms in MONDO
| Label |
Id |
Description |
|
pigmented nodular adrenocortical disease, primary, 2
|
MONDO_0012505 |
|
|
agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
|
MONDO_0012508 |
|
|
pigmented nodular adrenocortical disease, primary, 1
|
MONDO_0012509 |
|
|
dendritic cell deficiency
|
MONDO_0850812 |
|
|
hypotrichosis 2
|
MONDO_0007805 |
|
|
hypotrichosis simplex of the scalp
|
MONDO_0019575 |
|
|
obsolete hypotrichosis 4
|
MONDO_0007806 |
|
|
obsolete hypoplasia of teeth roots
|
MONDO_0007801 |
|
|
hypospadias 3, autosomal
|
MONDO_0007802 |
|
|
chromosome 18p deletion syndrome
|
MONDO_0007800 |
|
|
ichthyosis histrix, Lambert type
|
MONDO_0007809 |
|
|
ichthyosis hystrix
|
MONDO_0859383 |
|
|
hypoxanthine guanine phosphoribosyltransferase suppressor
|
MONDO_0007807 |
|
|
ichthyosis hystrix of Curth-Macklin
|
MONDO_0007808 |
|
|
obsolete immune suppression
|
MONDO_0007816 |
|
|
IgE responsiveness, atopic
|
MONDO_0007817 |
|
|
immune deficiency, familial variable
|
MONDO_0007814 |
|
|
obsolete immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist
|
MONDO_0007815 |
|
|
ichthyosis, lamellar, autosomal dominant
|
MONDO_0007812 |
|
|
superficial epidermolytic ichthyosis
|
MONDO_0007813 |
|
