All terms in MONDO
| Label |
Id |
Description |
|
renal hypoplasia, bilateral
|
MONDO_0019980 |
|
|
metastatic squamous cell carcinoma
|
MONDO_0044907 |
|
|
bilateral multicystic dysplastic kidney
|
MONDO_0019982 |
|
|
multicystic dysplastic kidney
|
MONDO_0015988 |
|
|
unilateral multicystic dysplastic kidney
|
MONDO_0019981 |
|
|
myopathy, congenital proximal, with minicore lesions
|
MONDO_0032937 |
|
|
basal ganglia calcification, idiopathic, 8, autosomal recessive
|
MONDO_0032938 |
|
|
rhizomelic limb shortening with dysmorphic features
|
MONDO_0032935 |
|
|
myopathy, congenital, with respiratory insufficiency and bone fractures
|
MONDO_0032936 |
|
|
chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant
|
MONDO_0032933 |
|
|
genitourinary and/or brain malformation syndrome
|
MONDO_0032934 |
|
|
mitochondrial DNA depletion syndrome 18
|
MONDO_0032932 |
|
|
obsolete viral human hepatitis
|
MONDO_0005343 |
|
|
intellectual developmental disorder, autosomal dominant 63, with macrocephaly
|
MONDO_0032939 |
|
|
hereditary persistence of fetal hemoglobin
|
MONDO_0020989 |
|
|
fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency
|
MONDO_0017336 |
|
|
inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency
|
MONDO_0017337 |
|
|
paranasal sinus mucoepidermoid carcinoma
|
MONDO_0044956 |
|
|
pyoderma gangrenosum-acne-suppurative hidradenitis syndrome
|
MONDO_0017332 |
|
|
maternal uniparental disomy of chromosome 13
|
MONDO_0019994 |
|
