Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Green
Phenotypes
- Megaloblastic anemia-1, Norwegian type, MIM#261100
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
|
Sources
-
Expert list
-
Expert Review Green
Phenotypes
- Lipoprotein glomerulopathy, MIM#611771
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Phenotypes
- Complement factor H deficiency, MIM#609814
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
|
Sources
-
Expert list
-
Expert Review Green
-
Victorian Clinical Genetics Services
Phenotypes
- Proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis, MIM#308990
- Dent disease, MIM#300009
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Green
Phenotypes
- Nephrotic syndrome, type 9, MIM#615573
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Green
Phenotypes
- Nephrotic syndrome, type 16, MIM#617783
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Phenotypes
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert Review Green
-
Literature
Phenotypes
- Nephrotic syndrome, type 18, MIM#618177
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert Review Green
-
Literature
Phenotypes
- Nephrotic syndrome, type 17, MIM#618176
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Green
Phenotypes
- Nephrotic syndrome, type 12, MIM#616892
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
X-LINKED: hemizygous mutation in males, biallelic mutations in females
|
Sources
-
Expert list
-
Expert Review Green
-
Victorian Clinical Genetics Services
Phenotypes
- Dent disease 2, MIM#300555
- Lowe syndrome, MIM#309000
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Phenotypes
- Glomerulosclerosis, focal segmental, 7, MIM#616002
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Phenotypes
- Nephrotic syndrome, type 20, MIM# 301028
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Green
Green List (high evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Green
-
Victorian Clinical Genetics Services
Tags
|
Amber
Amber List (moderate evidence)
|
|
0 reviews
|
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
|
Sources
-
Expert Review Amber
-
Victorian Clinical Genetics Services
Phenotypes
- {Glomerulosclerosis, focal segmental, 4, susceptibility to}, MIM#612551
Tags
|
Amber
Amber List (moderate evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Amber
Phenotypes
Tags
|
Amber
Amber List (moderate evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Amber
Tags
|
Amber
Amber List (moderate evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Amber
Phenotypes
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
|
Sources
-
Expert Review Red
-
Victorian Clinical Genetics Services
Phenotypes
- Brain small vessel disease 2, MIM#614483
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
Unknown
|
Sources
-
Expert Review Red
-
Victorian Clinical Genetics Services
Phenotypes
- Coenzyme Q10 deficiency, primary, 4, MIM#612016
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert Review Red
-
Victorian Clinical Genetics Services
Phenotypes
- Epidermolysis bullosa, junctional, with pyloric atresia, MIM#226730
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
|
Sources
-
Expert Review Red
-
Victorian Clinical Genetics Services
Phenotypes
- Familial partial lipodystrophy
- FSGS
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert Review Red
-
Literature
Phenotypes
- Nephrotic syndrome, type 19, MIM#618178
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Red
Phenotypes
- Nephrotic syndrome, type 13, MIM#616893
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert list
-
Expert Review Red
Phenotypes
Tags
|
Red
Red List (low evidence)
|
|
0 reviews
|
BIALLELIC, autosomal or pseudoautosomal
|
Sources
-
Expert Review Red
-
Victorian Clinical Genetics Services
Phenotypes
- Nephronophthisis 12, MIM#613820
Tags
|