Disease #01081 (MASA (MASA syndrome (mental retardation, aphasia, shuffling gait, adducted thumbs; CRASH syndrome)), OMIM:303350)
Official abbreviation |
MASA |
Name |
MASA syndrome (mental retardation, aphasia, shuffling gait, adducted thumbs; CRASH syndrome) |
OMIM ID |
303350 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
X-linked recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
L1CAM |
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) |
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