| Entry |
|
|---|
| Name |
|
|---|
| Type |
Loss of function
|
|---|
| Gene |
|
|---|
| Organism |
hsa_var Human gene variants (Homo sapiens)
|
|---|
| Variation |
|
|---|
| Network |
|
|---|
| Disease |
| H00646 | Odontoonychodermal dysplasia |
| H00781 | Schopf-Schulz-Passarge syndrome |
|
|---|
| Reference |
|
|---|
| Authors |
Yu M, Wong SW, Han D, Cai T |
|---|
| Title |
Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis. |
|---|
| Journal |
|
|---|
| Reference |
|
|---|
| Authors |
Martinez-Gil N, Ugartondo N, Grinberg D, Balcells S |
|---|
| Title |
Wnt Pathway Extracellular Components and Their Essential Roles in Bone Homeostasis. |
|---|
| Journal |
|
|---|
| LinkDB |
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|---|
