Experimental Factor Ontology
12089 terms(s) returned
Term Type: | Record: 151 to 200 of 12089 Records | Page: 4 of 242, First Previous Next Last | Show Records Per Page |
- ALG3-congenital disorder of glycosylation
- ALG6-congenital disorder of glycosylation 1C
- ALG8-congenital disorder of glycosylation
- ALG9-associated autosomal dominant polycystic kidney disease
- ALG9-congenital disorder of glycosylation
- ALS2-related motor neuron disease
- ALys amyloidosis
- AMED syndrome, digenic
- ANE syndrome
- AP-4 deficiency syndrome
- APC-related attenuated familial adenomatous polyposis
- AREDYLD syndrome
- ASAH1-related disorders
- ASAH1-related sphingolipidosis
- ATM-related cancer predisposition
- ATP1A3-associated neurological disorder
- ATP6AP2-related disorder
- ATR-X-related syndrome
- ATTRV122I amyloidosis
- AXIN2-related attenuated familial adenomatous polyposis
- Aagenaes syndrome
- Aarskog-Scott syndrome, X-linked
- Aase-Smith syndrome
- Abruzzo-Erickson syndrome
- Acanthamoeba infectious disease
- Achondroplasia
- Ackerman syndrome
- Acrodysostosis 1 with or without hormone resistance
- Acromicric dysplasia
- Acroosteolysis dominant type
- Acrootoocular syndrome
- Acropectorovertebral dysplasia
- Adams-Oliver syndrome
- Aeromonas hydrophila intestinal disease
- African iron overload
- Aicardi syndrome
- Aicardi-Goutieres syndrome
- Aicardi-Goutieres syndrome 1
- Aicardi-Goutieres syndrome 6
- Aicardi-Goutieres syndrome 7
- Aicardi-Goutieres syndrome 8
- Aicardi-Goutieres syndrome 9
- Al Kaissi syndrome
- Al-Gazali syndrome
- Alagille syndrome
- Alagille syndrome due to 20p12 microdeletion
- Alagille syndrome due to a JAG1 point mutation
- Alagille syndrome due to a NOTCH2 point mutation
- Aland island eye disease
- Alazami-Yuan syndrome