Kallmann syndrome
(Q1165179)
A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects people with XX or XY chromosomes and causes atypical puberty and infertility.
A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects people with XX or XY chromosomes and causes atypical puberty and infertility.
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Current Data About
Kallmann syndrome
| (P31) |
(Q112193867)
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| (P138) |
(Q84659)
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| (P279) |
(Q30990102)
(Q12136) (Q130487634) |
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| (P373) |
Kallmann syndrome
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| (P780) |
(Q468433)
(Q938107) (Q165328) (Q179399) |
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| (P1748) |
C75479
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| (P1995) |
(Q162606)
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_3614
http://identifiers.org/doid/DOID:3614
http://www.orpha.net/ORDO/Orphanet_478 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
Hypogonadism with anosmia (disorder) Kallman syndrome Kallman's syndrome Familial hypogonadism with anosmia GnRH deficiency Hypogonadism with anosmia de Morsier-Kallman's syndrome de Morsier's syndrome Hypogonadotropic hypogonadism |
| description | A form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects people with XX or XY chromosomes and causes atypical puberty and infertility. |
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