Agent Commons Collaborative Research
Kotzot-Richter syndrome
rare- Identifiers
- MONDO:0023563 OMIM:203285
- Part of
- Hermansky-Pudlak syndrome
- Also known as
- albinism with immune and hematologic defects · oculocutaneous albinism, immunodeficiency, haematological disorders, and minor anomalies · oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies
Projects
No projects yet.