All terms in MONDO
| Label |
Id |
Description |
|
chromosome 19q13.11 deletion syndrome, distal
|
MONDO_0700107 |
|
|
skin disease caused by bacterial infection, non-human animal
|
MONDO_0700109 |
|
|
syndromic X-linked intellectual disability 34
|
MONDO_0010501 |
|
|
intellectual disability, X-linked, syndromic 33
|
MONDO_0010500 |
|
|
letterer-Siwe disease
|
MONDO_0009519 |
|
|
Langerhans cell histiocytosis specific to childhood
|
MONDO_0017025 |
|
|
leprosy, susceptibility to, 3
|
MONDO_0009518 |
|
|
Donohue syndrome
|
MONDO_0009517 |
|
|
absence deformity of leg-cataract syndrome
|
MONDO_0009516 |
|
|
Norum disease
|
MONDO_0009515 |
|
|
Laurence-Moon syndrome
|
MONDO_0009514 |
|
|
laryngo-onycho-cutaneous syndrome
|
MONDO_0009513 |
|
|
junctional epidermolysis bullosa
|
MONDO_0017612 |
|
|
lethal Larsen-like syndrome
|
MONDO_0009512 |
|
|
Larsen-like syndrome, B3GAT3 type
|
MONDO_0009511 |
|
|
obsolete Laron syndrome with immunodeficiency
|
MONDO_0009510 |
|
|
intellectual disability, X-linked 105
|
MONDO_0010510 |
|
|
intellectual disability, X-linked, syndromic, Bain type
|
MONDO_0010512 |
|
|
vas deferens, congenital bilateral aplasia of, X-linked
|
MONDO_0010511 |
|
|
pyruvate dehydrogenase E3 deficiency
|
MONDO_0009529 |
|
