Category:Autosomal recessive diseases and disorders
Jump to navigation
Jump to search
Radiology: Ultrasound · X-ray · Computed tomography · Magnetic resonance | Anatomical pathology: Gross pathology · Histopathology | File format: Video recording |
genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop | |||||
Upload media | |||||
Instance of |
| ||||
---|---|---|---|---|---|
Subclass of | |||||
| |||||
English: For more information on autosomal recessive inheritance, see the articles Autosomes, Recessive gene and Dominance relationship.
Subcategories
This category has the following 59 subcategories, out of 59 total.
A
- Aldolase A deficiency (3 F)
- Alkaptonuria (5 F)
B
C
- Chediak-Higashi syndrome (4 F)
- Cockayne syndrome (2 F)
E
F
- Familial dysautonomia (5 F)
- Fanconi anemia (6 F)
- Fucosidosis (3 F)
G
- Gitelman syndrome (1 F)
- Greenberg dysplasia (4 F)
H
- Harlequin-type ichthyosis (12 F)
I
K
L
- LIG4 syndrome (1 F)
M
- Meckel syndrome (2 F)
- Methylmalonic acidemias (4 F)
N
- Nephronophthisis (1 F)
O
- Ochronosis (2 F)
- Omenn syndrome (1 F)
P
- Phenylketonuria (11 F)
- Pseudoxanthoma elasticum (3 F)
R
- Refsum disease (3 F)
S
T
U
W
Media in category "Autosomal recessive diseases and disorders"
The following 2 files are in this category, out of 2 total.
-
Herència gen Malaltia de Gaucher.png 511 × 471; 33 KB
-
Otozomalresesif.jpg 738 × 1,283; 83 KB