Disease #06379 (NEDCFSA (Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities), OMIM:618505)
Official abbreviation |
NEDCFSA |
Name |
Neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities |
OMIM ID |
618505 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
KDM6B |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
N/A |
Individuals
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