Disease #03429 (C3D (complement component 3 deficiency, autosomal recessive (C3D)), OMIM:613779)
Official abbreviation |
C3D |
Name |
complement component 3 deficiency, autosomal recessive (C3D) |
OMIM ID |
613779 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
17 |
Phenotype entries for this disease |
16 |
Associated with 1 gene |
C3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|