Search on: KALLMANN SYNDROME 
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Descriptor English:   Kallmann Syndrome 
Descriptor Spanish:   Síndrome de Kallmann 
Descriptor Portuguese:   Síndrome de Kallmann 
Synonyms English:   Anosmic Hypogonadism
Anosmic Idiopathic Hypogonadotropic Hypogonadism
Autosomal Dominant Form of Kallmann Syndrome
Autosomal Recessive Form of Kallmann Syndrome
Dysplasia Olfactogenitalis of De Morsier
Hypogonadotropic Hypogonadism and Anosmia
Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion)
Hypogonadotropic Hypogonadism-Anosmia Syndrome
Kallmann Syndrome 1
Kallmann Syndrome 2
Kallmann Syndrome 3
Kallmann Syndrome, Type 1, X-linked
Kallmann Syndrome, Type 3, Recessive
Kallmann's Syndrome
Anosmic Hypogonadisms
Hypogonadism, Anosmic
Hypogonadisms, Anosmic
Kallmanns Syndrome
Syndrome, Kallmann
Syndrome, Kallmann's  
Tree Number:   C12.706.316.096.750
C13.351.875.253.096.750
C16.131.939.316.096.750
C16.320.467
C19.391.119.096.750
C19.391.482.600
Definition English:   A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait. 
See Related English:   Gonadotropin-Releasing Hormone
Receptor, Fibroblast Growth Factor, Type 1
 
History Note English:   93 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DG diagnostic imaging DH diet therapy
DT drug therapy EC economics
EM embryology EN enzymology
EP epidemiology EH ethnology
ET etiology GE genetics
HI history IM immunology
ME metabolism MI microbiology
MO mortality NU nursing
PS parasitology PA pathology
PP physiopathology PC prevention & control
PX psychology RT radiotherapy
RH rehabilitation SU surgery
TH therapy UR urine
VE veterinary VI virology
Record Number:   30678 
Unique Identifier:   D017436 

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