All terms in MONDO
| Label |
Id |
Description |
|
XH antigen
|
MONDO_0010760 |
|
|
spermatogenic failure, Y-linked, 1
|
MONDO_0010763 |
|
|
partial chromosome Y deletion
|
MONDO_0015607 |
|
|
lymphoma, Hodgkin, Y-linked pseudoautosomal
|
MONDO_0010762 |
|
|
hearing loss, Y-linked 1
|
MONDO_0010764 |
|
|
nonsyndromic deafness, Y-linked
|
MONDO_0033304 |
|
|
mixed dust pneumoconiosis
|
MONDO_0022745 |
|
|
obsolete cochlear nerve deficiency
|
MONDO_0034733 |
|
|
chromosome 13p duplication
|
MONDO_0022746 |
|
|
non-neoplastic nevus
|
MONDO_0022749 |
|
|
obsolete angioedema, hereditary, type 1/2
|
MONDO_0007117 |
|
|
isolated anhidrosis with normal sweat glands
|
MONDO_0007118 |
|
|
autosomal recessive omodysplasia
|
MONDO_0009779 |
|
|
chromosome 18 mosaic monosomy
|
MONDO_0022755 |
|
|
Von Willebrand disease, X-linked form
|
MONDO_0010756 |
|
|
olivopontocerebellar atrophy II, autosomal recessive
|
MONDO_0009778 |
|
|
angioma serpiginosum, autosomal dominant
|
MONDO_0007115 |
|
|
vesicoureteral reflux, X-linked
|
MONDO_0010755 |
|
|
hereditary neurocutaneous angioma
|
MONDO_0007116 |
|
|
Oliver syndrome
|
MONDO_0009777 |
|
