Disease #01053 (HH1;KAL1 (hypogonadism, hypogonadotropic, type 1, with/without anosmia (Kallmann syndrome)), OMIM:308700)
| Official abbreviation |
HH1;KAL1 |
| Name |
hypogonadism, hypogonadotropic, type 1, with/without anosmia (Kallmann syndrome) |
| OMIM ID |
308700 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
KAL1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-10-17 21:44:29 +02:00 (CEST) |
Individuals
|