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
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