All terms in MONDO
| Label |
Id |
Description |
|
obsolete Glanzmann's thrombasthenia
|
MONDO_0010119 |
|
|
dysmyelination with jaundice
|
MONDO_0009137 |
|
|
dyskeratosis congenita, autosomal recessive 1
|
MONDO_0009136 |
|
|
anemia, congenital dyserythropoietic, type 1a
|
MONDO_0009135 |
|
|
myopathy, distal, 7, adult-onset, X-linked
|
MONDO_0024771 |
|
|
congenital dyserythropoietic anemia type 2
|
MONDO_0009134 |
|
|
autoinflammatory syndrome, familial, X-linked, Behcet-like 2
|
MONDO_0024770 |
|
|
Meier-Gorlin syndrome 1
|
MONDO_0009143 |
|
|
hypophosphatemic rickets and hyperparathyroidism
|
MONDO_0012795 |
|
|
familial thyroid dyshormonogenesis
|
MONDO_0010132 |
|
|
dystonia with Ringbinden
|
MONDO_0009142 |
|
|
thyroid hormone resistance, generalized, autosomal recessive
|
MONDO_0010131 |
|
|
retinitis pigmentosa 41
|
MONDO_0012796 |
|
|
torsion dystonia 2
|
MONDO_0009141 |
|
|
hypouricemia, renal, 2
|
MONDO_0012793 |
|
|
Pendred syndrome
|
MONDO_0010134 |
|
|
Silverman-Handmaker type dyssegmental dysplasia
|
MONDO_0009140 |
|
|
ANE syndrome
|
MONDO_0012794 |
|
|
thyroid dyshormonogenesis 2A
|
MONDO_0010133 |
|
|
hypertrophic cardiomyopathy 11
|
MONDO_0012799 |
|
