Disease #00776 (BFLS (Borjeson-Forssman-Lehmann syndrome (BFLS)), OMIM:301900)
| Official abbreviation |
BFLS |
| Name |
Borjeson-Forssman-Lehmann syndrome (BFLS) |
| OMIM ID |
301900 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PHF6 |
| Associated tissues |
- |
| Disease features |
deep-set eyes, large ears with large lobes; global developmental delay (HP:0001263); intellectual disability (HP:0001249); seizure (HP:0001250); hypotonia (HP:0001252); short stature (HP:0004322); obesity (HP:0001513); digital abnormalities (HP_0011297); tapering fingers, rather hypoplastic external genitalia with pubertal delay |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-01-03 20:06:20 +01:00 (CET) |
Individuals
|