Disease #01053 (HH1;KAL1 (hypogonadism, hypogonadotropic, type 1, with/without anosmia (HH-1, Kallmann syndrome, type 1 KAL-1))), OMIM:308700)

Official abbreviation HH1;KAL1
Name hypogonadism, hypogonadotropic, type 1, with/without anosmia (HH-1, Kallmann syndrome, type 1 KAL-1))
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 -
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00037755 - - - M no (China) Han Chinese - - - - HH1;KAL1 hypogonadotropic hypogonadism, anosmia or hyposmia, no mental retardation KAL1 KAL1 1 1 Fei Wang
00037757 - - - M - Belgium European - - - - HH1;KAL1 hypogonatropic hypogonadism, anosmy, cryptorchidism KAL1 KAL1 1 1 Cecile Libioulle
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