All terms in MONDO
| Label | Id | Description |
|---|---|---|
| metaphyseal chondrodysplasia, Pena type | MONDO_0009596 | |
| cartilage-hair hypoplasia | MONDO_0009595 | |
| obsolete inherited genitourinary tract anomalies | MONDO_0010594 | |
| obsolete Frontometaphyseal dysplasia | MONDO_0010593 | |
| membranoproliferative glomerulonephritis, X-linked | MONDO_0010596 | |
| Sertoli cell-only syndrome | MONDO_0010595 | |
| glycogen storage disease IXa1 | MONDO_0010598 | |
| glycogen storage disease due to liver phosphorylase kinase deficiency | MONDO_0020693 | |
| glutamyl ribose-5-phosphate storage disease | MONDO_0010597 | |
| granulomas, congenital cerebral | MONDO_0010599 | |
| benign angiitis of the central nervous system | MONDO_0022559 | |
| FG syndrome 1 | MONDO_0010590 | |
| focal dermal hypoplasia | MONDO_0010592 | |
| fingerprint body myopathy | MONDO_0010591 | |
| obsolete BEST1 retinopathy | MONDO_0022566 | |
| bhaskar jagannathan syndrome | MONDO_0022567 | |
| bidirectional tachycardia | MONDO_0022568 | |
| benign metastasizing leiomyoma | MONDO_0022560 | |
| brachydactyly absence of distal phalanges | MONDO_0022598 | |
| brachydactyly anonychia | MONDO_0022599 |