All terms in MONDO
| Label |
Id |
Description |
|
pulmonic stenosis
|
MONDO_0009938 |
|
|
varicella, severe recurrent
|
MONDO_0010919 |
|
|
familial primary pulmonary hypoplasia
|
MONDO_0009936 |
|
|
pulmonary hypertension, primary, autosomal recessive
|
MONDO_0009935 |
|
|
alveolar capillary dysplasia with misalignment of pulmonary veins
|
MONDO_0009934 |
|
|
congenital pulmonary lymphangiectasia
|
MONDO_0009933 |
|
|
enuresis, nocturnal, 1
|
MONDO_0010910 |
|
|
pulmonary bullae causing pneumothorax
|
MONDO_0009932 |
|
|
pulmonary atresia-intact ventricular septum syndrome
|
MONDO_0009931 |
|
|
fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement
|
MONDO_0010912 |
|
|
obsolete pulmonary arteriovenous malformation
|
MONDO_0009930 |
|
|
prolactin-producing pituitary gland adenoma
|
MONDO_0010911 |
|
|
carnitine palmitoyl transferase II deficiency, severe infantile form
|
MONDO_0010914 |
|
|
Caroli disease
|
MONDO_0010913 |
|
|
polycystic kidney disease 3 with or without polycystic liver disease
|
MONDO_0010916 |
|
|
autosomal dominant nonsyndromic hearing loss 4A
|
MONDO_0010915 |
|
|
anophthalmia plus syndrome
|
MONDO_0010930 |
|
|
craniosynostosis 4
|
MONDO_0010929 |
|
|
dwarfism, familial, with muscle spasms
|
MONDO_0010928 |
|
|
pyropoikilocytosis, hereditary
|
MONDO_0009948 |
|
