DiseaseID 8850
睾酮中毒症
disease
Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, ear
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Disease: 1Formula: 18Herb: 12Symptom: 7Target: 23Links: 61
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 8850
- Core Entity Id
- 65840
- Source Entity Count
- 1
- Preferred Name
- Testotoxicosis
- Name Cn
- 睾酮中毒症
- Name Pinyin
- Gao Tong Zhong Du Zheng
- Name En
- Testotoxicosis
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Endocrine System DiseasesFemale Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System DiseasesMale Urogenital Diseases; Neoplasms; Endocrine System DiseasesPathological Conditions, Signs and Symptoms
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the endocrine system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System DiseasesEndocrine System DiseasesNeoplasms; Male Urogenital Diseases; Endocrine System DiseasesPathological Conditions, Signs and Symptoms
- Hpo Class Name
- Abnormality of the endocrine system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, ear
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Testotoxicosis
Role
preferred
Name
Aromatase Excess Syndrome
Role
preferred
Name
Familial Male-Limited Precocious Puberty
Role
preferred
Name
Precocious Puberty
Role
preferred
Name
Precocious Puberty, Male-Limited
Role
preferred
Name
Central Precocious Puberty
Role
preferred
Name
Cryptogenic Sexual Precocity
Role
preferred
Name
Early Menarche
Role
preferred
Name
Familial Testotoxicosis
Role
preferred
Name
Leydig Cell Adenoma, Somatic, With Male-Limited Precocious Puberty
Role
preferred
Name
AEXS
Role
alias
Name
AROMATASE ACTIVITY, INCREASED
Role
alias
Name
Early Onset of Puberty
Role
alias
Name
Early Puberty
Role
alias
Name
FMPP
Role
alias
Name
Familial Gonadotropin-independent Male-limited Sexual Precocity
Role
alias
Name
Familial Gynecomastia, Due To Increased Aromatase Activity
Role
alias
Name
GYNECOMASTIA, FAMILIAL, DUE TO INCREASED AROMATASE ACTIVITY
Role
alias
Name
GYNECOMASTIA, HEREDITARY
Role
alias
Name
Male-limited Precocious Puberty
Role
alias
Name
Puberty, Precocious
Role
alias
Name
SEXUAL PRECOCITY, FAMILIAL, GONADOTROPIN-INDEPENDENT
Role
alias
Name
Sexual Precocity
Role
alias
Name
TESTOTOXICOSIS, FAMILIAL
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0000826
Herb
HBDIS002532HBDIS006609HBDIS008020HBDIS008023HBDIS008024HBDIS014309HBDIS018802HBDIS019323
Me Sh
D011629
Omim
139300176410
Umls
C0034013C0342549C1504412C1970109C2674612
Icd10
E30.1
Med Dra
1006365410063656
Sym Map
SMDE03632SMDE03842SMDE04954SMDE12391
Do Class
DOID:7
Dis Ge Net
C0034013C0271527C0342543C0342548C0342549C1504412C1970109C2674612
Orphanet
3000
Umls Sty
T033T047T191
Hpo Class
HP:0000818
Me Sh Class
C04C12C13C16C17C18C19C23
Etcm Disease
Aromatase Excess SyndromeCentral Precocious Puberty
Tcmbank Disease
1549523154241542803431399364360679217
Itcmdb Generated
ITX-DISEASE-459085662CD3ITX-DISEASE-4A0F7F32D66BITX-DISEASE-B99F69114023ITX-DISEASE-C26C88F3EAF9
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Aromatase Excess Syndrome Details pageDisease Central Precocious Puberty Details page
Do Class Name
disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the endocrine system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the endocrine system
Umls Disease Type
Disease or SyndromeFindingNeoplastic Process
Basic Information
Disease Name
Aromatase Excess Syndrome
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Endocrine diseases;Reproductive diseases
Disease Name
Central Precocious Puberty
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Endocrine diseases;Reproductive diseases
Disease Definition
Familial male limited precocious puberty (FMPP) is a gonadotropin-independent familial form of male-limited precocious puberty, generally presenting between 2-5 years of age as accelerated growth, earNCI2016_NICHD_1602D:Onset of sexual development, before the age of 8 years in females and before the age of 9 years in males.|NCI2016_CTCAE_1602D:A disorder characterized by unusually early development of secondary sexual features; the onset of sexual maturation begins usually before age 8 for girls and before age 9 for boys.|NCI2016_02D:Unusually early sexual maturity.|MSH2017_2016_08_12:Development of SEXUAL MATURATION in boys and girls at a chronological age that is 2.5 standard deviations below the mean age at onset of PUBERTY in the population. This early maturation of the hypothalamic-pituitary-gonadal axis results in sexual precocity, elevated serum levels of GONADOTROPINS and GONADAL STEROID HORMONES such as ESTRADIOL and TESTOSTERONE.|HPO2016_07_04:The onset of secondary sexual characteristics before a normal age. Although it is difficult to define normal age ranges because of the marked variation with which puberty begins in normal children, precocious puberty can be defined as the onset of puberty before the age of 8 years in girls or 9 years in boys. [HPO:probinson]|CSP2006:unusually early sexual maturity.
Me Sh Disease Class
Endocrine System DiseasesFemale Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System DiseasesMale Urogenital Diseases; Neoplasms; Endocrine System DiseasesPathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Endocrine System DiseasesEndocrine System DiseasesNeoplasms; Male Urogenital Diseases; Endocrine System DiseasesPathological Conditions, Signs and Symptoms
Umls Semantic Type Name
Disease or SyndromeFindingNeoplastic Process