All terms in MONDO
| Label |
Id |
Description |
|
combined oxidative phosphorylation deficiency 29
|
MONDO_0014781 |
|
|
hyperphosphatasia with intellectual disability syndrome 6
|
MONDO_0014780 |
|
|
obsolete progeroid syndrome
|
MONDO_0000146 |
|
|
obsolete premature aging syndrome
|
MONDO_0000145 |
|
|
VEXAS syndrome
|
MONDO_0026777 |
|
|
pregnancy loss, recurrent, susceptibility
|
MONDO_0000144 |
|
|
obsolete multiple mitochondrial dysfunctions syndrome
|
MONDO_0000143 |
|
|
obsolete retinopathy
|
MONDO_0000149 |
|
|
pulmonary fibrosis and/or bone marrow failure, telomere-related
|
MONDO_0000148 |
|
|
bone marrow disorder
|
MONDO_0003225 |
|
|
neoplastic polyp
|
MONDO_0021075 |
|
|
asperger syndrome, susceptibility to, 3
|
MONDO_0012119 |
|
|
obsolete multiple congenital anomalies-hypotonia-seizures syndrome
|
MONDO_0000142 |
|
|
mosaic variegated aneuploidy syndrome
|
MONDO_0000141 |
|
|
obsolete MONDO:0000140
|
MONDO_0000140 |
|
|
developmental and epileptic encephalopathy, 85, with or without midline brain defects
|
MONDO_0026771 |
|
|
restless legs syndrome, susceptibility to, 2
|
MONDO_0012135 |
|
|
brachydactyly type A1D
|
MONDO_0014798 |
|
|
lymphatic malformation 6
|
MONDO_0014797 |
|
|
carnitine palmitoyl transferase II deficiency, neonatal form
|
MONDO_0012136 |
|
