All terms in MONDO
| Label |
Id |
Description |
|
ectodermal dysplasia with intellectual disability and syndactyly
|
MONDO_0010955 |
|
|
Charcot-Marie-Tooth disease with ptosis and parkinsonism
|
MONDO_0007312 |
|
|
cardiac arrhythmia, ankyrin-B-related
|
MONDO_0010958 |
|
|
respiratory underresponsiveness to hypoxia and hypercapnia
|
MONDO_0009972 |
|
|
agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformations
|
MONDO_0010957 |
|
|
Charcot-Marie-Tooth disease, Guadalajara neuronal type
|
MONDO_0007310 |
|
|
respiratory distress syndrome in premature infants
|
MONDO_0009971 |
|
|
renal tubular dysgenesis of genetic origin
|
MONDO_0009970 |
|
|
renal tubular dysgenesis
|
MONDO_0017609 |
|
|
van den Ende-Gupta syndrome
|
MONDO_0010959 |
|
|
late-onset junctional epidermolysis bullosa
|
MONDO_0019309 |
|
|
cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies
|
MONDO_0010970 |
|
|
hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome
|
MONDO_0010972 |
|
|
obsolete immune deficiency with skin involvement
|
MONDO_0019305 |
|
|
infundibulopelvic stenosis-multicystic kidney syndrome
|
MONDO_0010971 |
|
|
nephrotic syndrome, type 2
|
MONDO_0010974 |
|
|
junctional epidermolysis bullosa inversa
|
MONDO_0019308 |
|
|
generalized junctional epidermolysis bullosa non-Herlitz type
|
MONDO_0019307 |
|
|
autosomal dominant nonsyndromic hearing loss 5
|
MONDO_0010973 |
|
|
Davenport-Donlan syndrome
|
MONDO_0022932 |
|
