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hypogonadotropic hypogonadism 3 with or without anosmia (DOID:0090092)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1)
Parent Terms Term With Siblings Child Terms
Kallmann syndrome +     
Brachytelephalangy Characteristic Facies Kallmann 
hypogonadotropic hypogonadism 1 with or without anosmia  
hypogonadotropic hypogonadism 2 with or without anosmia +   
hypogonadotropic hypogonadism 3 with or without anosmia  
A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the PROKR2 gene on chromosome 20p12, sometimes in association with mutation in another gene. (DO)
hypogonadotropic hypogonadism 4 with or without anosmia  
Hypogonadotropic Hypogonadism and Anosmia, Autosomal Dominant  
Kallmann Syndrome 5  
Kallmann Syndrome 6  
Spastic Paraplegia with Kallmann Syndrome 

Exact Synonyms: HH3 ;   Kallmann syndrome 3 ;   Kallmann syndrome type 3, recessive
Narrow Synonyms: hypogonadotropic hypogonadism 3 without anosmia
Primary IDs: OMIM:244200
Alternate IDs: RDO:9003766
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/17054399, https://www.ncbi.nlm.nih.gov/pubmed/18559922

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.