Hypogonadotropic hypogonadism 1 with or without anosmia
Hypogonadotropic hypogonadism 1 with or without anosmia
Definition
The X-linked inherited form of Kallmann syndrome caused by mutation of the KAL1 gene mapped to chromosome Xp22.3.
Also known as ANOS1 hypogonadotropic hypogonadism, hypogonadotropic hypogonadism 1 with or without anosmia, hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive, hypogonadotropic hypogonadism caused by mutation in ANOS1 — per MONDO
Also identified as
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Endocrine gland | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Gonad | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Gonad | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Reproductive system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Reproductive system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |