Disease #00146 (MATINS;MHA;BDPLT6 (macrothrombocytopenia, granulocyte inclusions with/without nephritis or sensorineural hearing loss (MATINS, May-Hegglin anomaly (MHA), bleeding disorder platelet type 6 (BDPLT-6))), OMIM:155100)
Official abbreviation |
MATINS;MHA;BDPLT6 |
Name |
macrothrombocytopenia, granulocyte inclusions with/without nephritis or sensorineural hearing loss (MATINS, May-Hegglin anomaly (MHA), bleeding disorder platelet type 6 (BDPLT-6)) |
OMIM ID |
155100 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
37 |
Phenotype entries for this disease |
36 |
Associated with 1 gene |
MYH9 |
Associated tissues |
- |
Disease features |
autosomal dominant |
Remarks |
- |
Date created |
2013-06-12 11:18:33 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|