- Rare
Diseases (ORD). This
means that
Iridogoniodysgenesis,
dominant type, or a
subtype of
Iridogoniodysgenesis,
dominant type,
affects less than 200...
-
Congenital hypothyroidism 2 PAX9 STHAG3 3.3 FOXC1
Axenfeld syndrome 3
Iridogoniodysgenesis,
dominant type FOXC2 Lymphedema–distichiasis
syndrome FOXE1 Bamforth–Lazarus...
-
phenotypes including primary congenital glaucoma,
autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld–Rieger
syndrome type 3. FOXC1
mutations are...
-
Congenital hypothyroidism 2 PAX9 STHAG3 3.3 FOXC1
Axenfeld syndrome 3
Iridogoniodysgenesis,
dominant type FOXC2 Lymphedema–distichiasis
syndrome FOXE1 Bamforth–Lazarus...
-
Iodine antenatal infection Iodine deficiency Iophobia Iridocy****is
Iridogoniodysgenesis,
dominant type Iris
dysplasia hypertelorism deafness Iritis Iron...
- 610799; IRAK4 IRAK4 deficiency; 607676; IRAK4
Iridogoniodysgenesis, type 1; 601631; FOXC1
Iridogoniodysgenesis, type 2; 137600; PITX2 Iris
hypoplasia and...
- in this gene are ****ociated with Axenfeld-Rieger
syndrome (ARS),
iridogoniodysgenesis syndrome (IGDS), and
sporadic cases of
Peters anomaly. This protein...
