Diseases Name | Mondo ID | Associated Targets | Direct Associated Targets | Rare |
---|---|---|---|---|
Cystathioninuria | MONDO:0009058 | |||
Pilarowski-Bjornsson syndrome | MONDO:0060568 | |||
Microcephaly 22, primary, autosomal recessive | MONDO:0054805 | |||
Cone dystrophy, retinal 3A | ||||
Retinitis pigmentosa 57 | MONDO:0013315 | |||
Alport syndrome, autosomal recessive | ||||
Hematuria, benign familial | MONDO:0007709 | |||
Alport syndrome, autosomal dominant | ||||
Complement component 2 deficiency | MONDO:0009006 | |||
Ehlers-Danlos syndrome, vascular type | MONDO:0017314 |