All terms in MONDO
| Label |
Id |
Description |
|
superior limbic keratoconjunctivitis
|
MONDO_0019504 |
|
|
obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome
|
MONDO_0019506 |
|
|
extragonadal non-dysgerminomatous germ cell tumor
|
MONDO_0020539 |
|
|
short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies
|
MONDO_0859198 |
|
|
developmental delay with or without intellectual impairment or behavioral abnormalities
|
MONDO_0859199 |
|
|
Ehlers-Danlos syndrome, autosomal dominant, type unspecified
|
MONDO_0007528 |
|
|
elastosis perforans serpiginosa
|
MONDO_0007529 |
|
|
Boudin-Mortier syndrome
|
MONDO_0859194 |
|
|
Usmani-Riazuddin syndrome, autosomal recessive
|
MONDO_0859196 |
|
|
autosomal dominant Ehlers-Danlos syndrome, vascular type
|
MONDO_0007524 |
|
|
intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies
|
MONDO_0859197 |
|
|
Ehlers-Danlos syndrome, arthrochalasis type
|
MONDO_0007525 |
|
|
neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities
|
MONDO_0859190 |
|
|
Ehlers-Danlos syndrome, classic type
|
MONDO_0007522 |
|
|
biliary, renal, neurologic, and skeletal syndrome
|
MONDO_0859191 |
|
|
Ehlers-Danlos syndrome, hypermobility type
|
MONDO_0007523 |
|
|
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
|
MONDO_0007520 |
|
|
neuroocular syndrome
|
MONDO_0859193 |
|
|
obsolete egasyn
|
MONDO_0007521 |
|
|
obsolete rare skin disease
|
MONDO_0019519 |
|