All terms in MONDO
| Label |
Id |
Description |
|
obsolete Addison disease
|
MONDO_0009410 |
|
|
pyloric stenosis, infantile hypertrophic, 4
|
MONDO_0010411 |
|
|
alopecia, androgenetic, 2
|
MONDO_0010410 |
|
|
intellectual disability, X-linked 95
|
MONDO_0010413 |
|
|
X-linked intellectual disability-craniofacioskeletal syndrome
|
MONDO_0010412 |
|
|
hypophosphatemia, renal, with intracerebral calcifications
|
MONDO_0009429 |
|
|
obsolete childhood hypophosphatasia
|
MONDO_0009428 |
|
|
obsolete infantile hypophosphatasia
|
MONDO_0009427 |
|
|
X-linked non progressive cerebellar ataxia
|
MONDO_0010404 |
|
|
hypoparathyroidism-retardation-dysmorphism syndrome
|
MONDO_0009426 |
|
|
albinism-hearing loss syndrome
|
MONDO_0010403 |
|
|
hypomandibular faciocranial dysostosis
|
MONDO_0009425 |
|
|
chromosome Xp11.22 duplication syndrome
|
MONDO_0010406 |
|
|
Bartter disease type 2
|
MONDO_0009424 |
|
|
prostate cancer, hereditary, X-linked 2
|
MONDO_0010405 |
|
|
hypokalemic alkalosis, familial, with specific renal tubulopathy
|
MONDO_0009423 |
|
|
syndactyly-telecanthus-anogenital and renal malformations syndrome
|
MONDO_0010408 |
|
|
hypohidrosis with abnormal palmar dermal Ridges
|
MONDO_0009422 |
|
|
intellectual disability, X-linked syndromic, Turner type
|
MONDO_0010407 |
|
|
hypogonadism, male
|
MONDO_0009421 |
|
