All terms in MONDO
| Label |
Id |
Description |
|
grouped pigmentation of the retina
|
MONDO_0009311 |
|
|
psoriasis 11, susceptibility to
|
MONDO_0012959 |
|
|
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2
|
MONDO_0009310 |
|
|
microvascular complications of diabetes, susceptibility to, 7
|
MONDO_0012971 |
|
|
febrile seizures, familial, 10
|
MONDO_0012972 |
|
|
osteopathia striata with cranial sclerosis
|
MONDO_0010310 |
|
|
microvascular complications of diabetes, susceptibility to, 6
|
MONDO_0012970 |
|
|
autosomal dominant nonsyndromic hearing loss 3B
|
MONDO_0012975 |
|
|
radial ray deficiency, X-linked
|
MONDO_0010312 |
|
|
autosomal dominant nonsyndromic hearing loss 2B
|
MONDO_0012976 |
|
|
Becker muscular dystrophy
|
MONDO_0010311 |
|
|
polymicrogyria, bilateral perisylvian, X-linked
|
MONDO_0010314 |
|
|
inflammatory bowel disease 26
|
MONDO_0012973 |
|
|
autosomal dominant nonsyndromic hearing loss 59
|
MONDO_0012974 |
|
|
intellectual disability, X-linked 63
|
MONDO_0010313 |
|
|
foot rot
|
MONDO_0024935 |
|
|
mumps infectious disease
|
MONDO_0000989 |
|
|
discharging ear
|
MONDO_0000988 |
|
|
cholesterolosis of gallbladder
|
MONDO_0000987 |
|
|
prostate squamous cell carcinoma
|
MONDO_0000993 |
|
