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Terminology chevron_right Concepts chevron_right 722944006

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722944006
The component that hold information about this concept.
Congenital hypogonadotropic hypogonadism (disorder)
Congenital hypogonadotropic hypogonadism
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Congenital hypogonadotropic hypogonadism (disorder)

SCTID: 722944006, Defined, Active


722944006|Congenital hypogonadotropic hypogonadism (disorder)|
  • en Congenital hypogonadotropic hypogonadism
  • en Congenital hypogonadotropic hypogonadism (disorder)

722944006 |Congenital hypogonadotropic hypogonadism (disorder)|

=== 33927004 |Hypogonadotropic hypogonadism (disorder)| +
    66091009 |Congenital disease (disorder)|
        { 363698007 |Finding site (attribute)| = 304041004 |Gonadal endocrine structure (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
        { 363698007 |Finding site (attribute)| = 52618001 |Structure of pars distalis of pituitary (body structure)|,
          246454002 |Occurrence (attribute)| = 255399007 |Congenital (qualifier value)| }
Active

3334001015 - Congenital hypogonadotropic hypogonadism (en) View

3334001015
en
Synonym (core metadata concept)
Congenital hypogonadotropic hypogonadism
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

3334000019 - Congenital hypogonadotropic hypogonadism (disorder) (en) View

3334000019
en
Fully specified name (core metadata concept)
Congenital hypogonadotropic hypogonadism (disorder)
900000000000448009 |Entire term case insensitive (core metadata concept)|
Preferred
True

66091009 View

66091009
Congenital disease (disorder)
Congenital disease
900000000000073002 |Sufficiently defined by necessary conditions definition status (core metadata concept)|
True

33927004 View

33927004
Hypogonadotropic hypogonadism (disorder)
Kallman syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

782917007 View

782917007
Familial adrenal hypoplasia with absent pituitary luteinizing hormone (disorder)
Familial adrenal hypoplasia miniature type
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

785722006 View

785722006
Obesity due to leptin receptor gene deficiency (disorder)
Obesity due to leptin receptor gene deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

770680004 View

770680004
Prader-willi-like syndrome (disorder)
Prader-willi-like syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

770941005 View

770941005
Alopecia, progressive neurological defect, endocrinopathy syndrome (disorder)
Ane syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

773665006 View

773665006
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural hearing loss, dysmorphism syndrome (disorder)
Hypogonadotropic hypogonadism, severe microcephaly, sensorineural deafness, dysmorphism syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

764959000 View

764959000
Intellectual disability, myopathy, short stature, endocrine defect syndrome (disorder)
Chudley rozdilsky syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

724174003 View

724174003
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome (disorder)
Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

724281002 View

724281002
Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome (disorder)
Bosma henkin christiansen syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

733113002 View

733113002
Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)
Chang davidson carlson syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

721842008 View

721842008
Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder)
Salti salem syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

722380003 View

722380003
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder)
Martsolf syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

700150001 View

700150001
Congenital leptin deficiency (disorder)
Congenital leptin deficiency
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

89392001 View

89392001
Prader-willi syndrome (disorder)
Prader-willi syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

93559003 View

93559003
Hypogonadism with anosmia (disorder)
Kallman syndrome
900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|
True

ExtendedMap object (8cac5da4-0fcb-5c3f-810f-bd497b1b3308) View

447562003 |Icd-10 complex map reference set (foundation metadata concept)|
E23.0
TRUE
ALWAYS E23.0
447561005 |Snomed ct source code to target map code correlation not specified (foundation metadata concept)|
447637006 |Map source concept is properly classified (foundation metadata concept)|
esc