All terms in MONDO
| Label |
Id |
Description |
|
pleomorphic carcinoma
|
MONDO_0003573 |
|
|
bladder sarcomatoid transitional cell carcinoma
|
MONDO_0850347 |
|
|
bladder small cell carcinoma
|
MONDO_0850348 |
|
|
obsolete genetic chronic primary adrenal insufficiency
|
MONDO_0020999 |
|
|
obsolete autoinflammatory syndrome with immune deficiency
|
MONDO_0017369 |
|
|
hereditary acrokeratotic poikiloderma, Weary type
|
MONDO_0017365 |
|
|
Kindler syndrome
|
MONDO_0008260 |
|
|
spinocerebellar ataxia, autosomal recessive 31
|
MONDO_0030323 |
|
|
obsolete kindler syndrome
|
MONDO_0017367 |
|
|
obsolete systemic disease with skin involvement
|
MONDO_0017368 |
|
|
congenital rubella syndrome
|
MONDO_0017361 |
|
|
neuralgic amyotrophy
|
MONDO_0017362 |
|
|
idiopathic chronic eosinophilic pneumonia
|
MONDO_0017363 |
|
|
POEMS syndrome
|
MONDO_0017364 |
|
|
spinocerebellar ataxia, autosomal recessive 30
|
MONDO_0030318 |
|
|
cardiomyopathy, familial hypertrophic, 28
|
MONDO_0030317 |
|
|
vitamin B12-unresponsive methylmalonic acidemia type mut0
|
MONDO_0017360 |
|
|
inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive
|
MONDO_0030314 |
|
|
encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10
|
MONDO_0030313 |
|
|
lymphatic malformation 11
|
MONDO_0030316 |
|
