Experimental Factor Ontology
937 terms(s) returned
| Term Type: | Record: 1 to 50 of 937 Records | Page: 1 of 19, First Previous Next Last | Show Records Per Page |
- MAN1B1-congenital disorder of glycosylation
- MASA syndrome
- MASS syndrome
- MED12-related intellectual disability syndrome
- MEDNIK syndrome
- MEGF10-related myopathy
- MEHMO syndrome
- MELAS syndrome
- MEND syndrome
- MERRF syndrome
- MGAT2-congenital disorder of glycosylation
- MHC class I deficiency
- MHC class II deficiency
- MIRAGE syndrome
- MIT family translocation renal cell carcinoma
- MKKS-related ciliopathy
- MME-related autosomal dominant Charcot Marie Tooth disease type 2
- MMEP syndrome
- MOGS-congenital disorder of glycosylation
- MOMO syndrome
- MORM syndrome
- MPDU1-congenital disorder of glycosylation
- MPI-congenital disorder of glycosylation
- MRCS syndrome
- MYH7-related skeletal myopathy
- MYPN-related myopathy
- Machado-Joseph disease
- Machado-Joseph disease type 1
- Machado-Joseph disease type 2
- Machado-Joseph disease type 3
- Madelung deformity
- Madelung deformity, bilateral
- Madelung deformity, unilateral
- Madras motor neuron disease
- Maffucci syndrome
- Majeed syndrome
- Malan overgrowth syndrome
- Marbach-Schaaf neurodevelopmental syndrome
- Marden-Walker syndrome
- Marfan and Marfan-related disorder
- Marfan syndrome
- Marie Unna hereditary hypotrichosis
- Marin-Amat syndrome
- Marinesco-Sjogren syndrome
- Marshall syndrome
- Marshall-Smith syndrome
- Martsolf syndrome
- Martsolf syndrome 2
- Matthew-Wood syndrome
- Mauriac syndrome
