Experimental Factor Ontology
512 terms(s) returned
| Term Type: | Record: 1 to 50 of 512 Records | Page: 1 of 11, First Previous Next Last | Show Records Per Page |
- D,L-2-hydroxyglutaric aciduria
- D-2-hydroxyglutaric aciduria
- D-glyceric aciduria
- DDOST-congenital disorder of glycosylation
- DDX41-related hematologic malignancy predisposition syndrome
- DEGCAGS syndrome
- DEND syndrome
- DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
- DICER1-related tumor predisposition
- DK1-congenital disorder of glycosylation
- DKC1-related disorder
- DNA ligase IV deficiency
- DOCK2 deficiency
- DOORS syndrome
- DPAGT1-congenital disorder of glycosylation
- DPH5-related diphthamide-deficiency syndrome
- DPM3-congenital disorder of glycosylation
- DYRK1A-related intellectual disability syndrome
- DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion
- Dahlberg-Borer-Newcomer syndrome
- Dandy-Walker malformation-postaxial polydactyly syndrome
- Darier disease
- DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion
- DeSanto-Shinawi syndrome
- DeSanto-Shinawi syndrome due to WAC point mutation
- Delpire-McNeill syndrome
- Dent disease
- Dent disease type 1
- Dent disease type 2
- Denys-Drash syndrome
- Desbuquois dysplasia
- Desbuquois dysplasia 2
- Diamond-Blackfan anemia
- Dianzani autoimmune lymphoproliferative disease
- Dias-Logan syndrome
- Donnai-Barrow syndrome
- Donohue syndrome
- Dorfman-Chanarin disease
- Dowling-Degos disease
- Dowling-Degos disease 1
- Doyne honeycomb retinal dystrophy
- Dravet syndrome
- Duane retraction syndrome
- Duane retraction syndrome 3 with or without deafness
- Duane-radial ray syndrome
- Dubin-Johnson syndrome
- Dubowitz syndrome
- Duchenne muscular dystrophy
- Dworschak-Punetha neurodevelopmental syndrome
- Dyggve-Melchior-Clausen disease
