All terms in MONDO
| Label |
Id |
Description |
|
mitochondrial complex 1 deficiency, nuclear type 17
|
MONDO_0032622 |
|
|
obsolete short rib-polydactyly syndrome, Verma-Naumoff type
|
MONDO_0019664 |
|
|
obsolete Y chromosome number anomaly
|
MONDO_0017005 |
|
|
mitochondrial complex 1 deficiency, nuclear type 15
|
MONDO_0032620 |
|
|
spondyloepimetaphyseal dysplasia, PAPSS2 type
|
MONDO_0019666 |
|
|
Pfeiffer syndrome type 3
|
MONDO_0019661 |
|
|
Pfeiffer syndrome type 2
|
MONDO_0019660 |
|
|
obsolete short rib-polydactyly syndrome, Saldino-Noonan type
|
MONDO_0019663 |
|
|
obsolete X chromosome number anomaly with female phenotype
|
MONDO_0017000 |
|
|
obsolete X chromosome number anomaly with male phenotype
|
MONDO_0017001 |
|
|
short rib-polydactyly syndrome, Majewski type
|
MONDO_0019662 |
|
|
mitochondrial complex 1 deficiency, nuclear type 13
|
MONDO_0032618 |
|
|
mitochondrial complex 1 deficiency, nuclear type 14
|
MONDO_0032619 |
|
|
mitochondrial complex 1 deficiency, nuclear type 10
|
MONDO_0032616 |
|
|
mitochondrial complex 1 deficiency, nuclear type 11
|
MONDO_0032617 |
|
|
epidermodysplasia verruciformis, susceptibility to, 2
|
MONDO_0032614 |
|
|
mitochondrial complex 1 deficiency, nuclear type 9
|
MONDO_0032615 |
|
|
mitochondrial complex 1 deficiency, nuclear type 7
|
MONDO_0032612 |
|
|
guanylate kinase 3
|
MONDO_0007689 |
|
|
mitochondrial complex 1 deficiency, nuclear type 8
|
MONDO_0032613 |
|
