All terms in MONDO
| Label |
Id |
Description |
|
distal arthrogryposis type 2B1
|
MONDO_0020820 |
|
|
Sheldon-hall syndrome
|
MONDO_0011128 |
|
|
congenital anomaly of the inferior vena cava
|
MONDO_0019830 |
|
|
congenital anomaly of the coronary sinus
|
MONDO_0019831 |
|
|
hypopigmentation, organomegaly, and delayed myelination and development
|
MONDO_0032805 |
|
|
trichothiodystrophy 7, nonphotosensitive
|
MONDO_0032806 |
|
|
palmoplantar keratoderma, punctate type 1A
|
MONDO_0007858 |
|
|
punctate palmoplantar keratoderma type 1
|
MONDO_0019332 |
|
|
immunodeficiency 64
|
MONDO_0032803 |
|
|
palmoplantar keratoderma i, striate, focal, or diffuse
|
MONDO_0007859 |
|
|
ectodermal dysplasia 15, hypohidrotic/hair type
|
MONDO_0032804 |
|
|
palmoplantar keratoderma-esophageal carcinoma syndrome
|
MONDO_0007856 |
|
|
erythrokeratodermia variabilis et progressiva 6
|
MONDO_0032801 |
|
|
keratosis palmaris et plantaris-clinodactyly syndrome
|
MONDO_0007857 |
|
|
hearing loss, autosomal dominant 37
|
MONDO_0032802 |
|
|
keratolytic winter erythema
|
MONDO_0007854 |
|
|
keratosis, familial actinic
|
MONDO_0007855 |
|
|
robinow syndrome, autosomal recessive 2
|
MONDO_0032800 |
|
|
palmoplantar keratoderma-deafness syndrome
|
MONDO_0007852 |
|
|
diaphragmitis
|
MONDO_0020830 |
|
