Disease #00191 (AMD2A (dysplasia, acromesomelic, type 2A, Grebe), OMIM:200700)
Official abbreviation |
AMD2A |
Name |
dysplasia, acromesomelic, type 2A, Grebe |
OMIM ID |
200700 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
GDF5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-09-08 14:51:28 +02:00 (CEST) |
Date last edited |
2021-12-16 17:35:12 +01:00 (CET) |
Individuals
|