Mondo Disease Ontology
5908 terms(s) returned
| Term Type: | Record: 301 to 350 of 5908 Records | Page: 7 of 119, First Previous Next Last | Show Records Per Page |
- ALG6
- ALG6-congenital disorder of glycosylation 1C
- ALG8
- ALG8-congenital disorder of glycosylation
- ALG9
- ALG9-associated autosomal dominant polycystic kidney disease
- ALG9-congenital disorder of glycosylation
- ALK
- ALK+ histiocytosis
- ALK-negative anaplastic large cell lymphoma
- ALK-positive anaplastic large cell lymphoma
- ALK-positive large B-cell lymphoma
- ALKBH8
- ALMS1
- ALMS1
- ALOX12B
- ALOX5
- ALOX5AP
- ALOXE3
- ALPI-related inflammatory bowel disease
- ALPK1
- ALPK3
- ALPL
- ALPL-related autosomal dominant hypophosphatasia
- ALPL-related autosomal recessive hypophosphatasia
- ALS2
- ALS2-related motor neuron disease
- ALX1
- ALX3
- ALX4
- ALys amyloidosis
- AMACR
- AMBN
- AMED syndrome, digenic
- AMELX
- AMER1
- AMFR
- AMH
- AMHR2
- AMMECR1
- AMN
- AMN
- AMPD1
- AMPD2
- AMPD3
- AMT
- ANAPC1
- ANAPC7
- ANE syndrome
- ANG
