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Kallmann s syndrome
LE WE PMID CA
Kallmann s syndrome3670Kallmann Syndrom

11 hydoxylase

17 20 Desmolase

17 alpha hydroxylase 17 20 lyase

17 beta hydroxysteroid dehydrogenase

20 22 Desmolase

21 hydroxylase deficiency

3 beta hydroxysteroid dehydrogenase2

3 beta hydroxysteroid dehydrogenase3

5 alpha Reductase

Adrenal gland (Hyperplasia congenital)

Albinism

AMH

AMHR2

Androgen insensitivity syndrome

Androgens (Hypogonadotropic hypogonadism)

Axon guidance

Campomelic dysplasia

Congenital adrenal hyperplasia

Congenital fibrosis of the extraocular muscles type1

Corpus callosum

CYP19A1 Aromatase

DAX1 NR0B1

Denys Drash syndrome

Duane retraction syndrome

Folliculogenesis

Frasier s syndrome

GPR54 KISS1R

Growth cone

GS alpha

Hedgehog

HESX1

Horizontal gaze palsy with progressive scoliosis

HSD17B3

Hypophysis (Development)

Infertility

INSL3 Insulin like 3 Relaxin like factor

Joubert s syndrome

KAL

Kallmann s syndrome

L1 syndrome

Leptin

LHX3 Lim3

LHX4

McCune Albright syndrome

NR5A1 SF1

P450 side chain cleavage

PC1

Pituitary gland (Insufficiency Panhypopituitarism)

Pontine tegmental cap dysplasia

PROK1

PROK2

Prokineticin

PROP1

Puberty (Delayed)

Puberty (Precocious)

Receptor (Androgen)

Receptor (Estrogen)

Receptor (FGFR1)

Receptor (FSH)

Receptor (Glucocorticoid)

Receptor (GnRH)

Receptor (LH)

SOX9

Spermatogenesis and spermatozoon

Sry

StAR

Steroid hormones (Synthesis)

TAC3

TACR3

Testis (Development)

WT1

2002  
1
Kallmann syndrome: adhesion, afferents, and anosmia.
[12062015] Neuron 34(5): 675-8 (2002)
2002  
2
Genetic causes of human reproductive disease.
[12050198] J Clin Endocrinol Metab 87(6): 2447-54 (2002)
2002  
3
Clinical review 148: Monogenic disorders of puberty.
[12050203] J Clin Endocrinol Metab 87(6): 2481-94 (2002)
2007  
4
A mutation in the fibroblast growth factor receptor 1 gene causes fully penetrant normosmic isolated hypogonadotropic hypogonadism.
[17200176] J Clin Endocrinol Metab 92(3): 1155-8 (2007)
2010  
5
Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships.
[20207726] Eur J Endocrinol 162(5): 835-51 (2010)
2004  
6
New insights in the genetics of isolated hypogonadotropic hypogonadism.
[15554891] Eur J Endocrinol 151 Suppl 3(-): U83-8 (2004)
2010  
7
2010  
8
The role of prokineticins in the pathogenesis of hypogonadotropic hypogonadism.
[20502053] Neuroendocrinology 91(4): 283-90 (2010)

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All Medline data shown were primarily retrieved from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.


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