Precocious puberty

Symptom Information:

Symptom ID: HPO:0000826
Synonyms:
Precocious puberty (disorder) [Orphanet:41750]
Precocious sexual development (disorder) [Orphanet:41750]
Precocious Puberty [Orphanet:41750]
Precocious puberty [OMIM:Precocious puberty]
Precocious puberty [Orphanet:41750]
True precocious puberty [Orphanet:41750]
Precocious puberty [MedDRA:10058084]
Accelerated sexual maturation [MedDRA:10058084]
Accelerated sexual maturity [MedDRA:10058084]
Early puberty [MedDRA:10058084]
Female sex maturation accelerated [MedDRA:10058084]
Male sex maturation accelerated [MedDRA:10058084]
Maturation sex accelerated [MedDRA:10058084]
Precocious puberty NOS [MedDRA:10058084]
Precocious sexual development and puberty, not elsewhere classified [MedDRA:10058084]
Premature adrenarche [MedDRA:10058084]
Premature thelarche [MedDRA:10058084]
Puberty precocious [MedDRA:10058084]
Sex maturation female accelerated [MedDRA:10058084]
Sex maturation male accelerated [MedDRA:10058084]
True precocious puberty [MedDRA:10058084]
Premature pubarche [MedDRA:10058084]
Central precocious puberty [MedDRA:10058084]
Early puberty [OMIM:Early puberty]
Precocious puberty (less common) [OMIM:Precocious puberty (less common)]
Premature pubarche (in 1 female patient) [OMIM:Premature pubarche (in 1 female patient)]
Premature pubarche (in some patients) [OMIM:Premature pubarche (in some patients)]
Quality:
Cross references:
HPO:0100000 "Early onset of puberty" [Orphanet:41750]
Orphanet:41750 "Precocious puberty" [Orphanet:41750]
OMIM: "Precocious puberty" [OMIM:Precocious puberty]
OMIM: "Early puberty" [OMIM:Early puberty]
OMIM: "Precocious puberty (less common)" [OMIM:Precocious puberty (less common)]
OMIM: "Premature pubarche (in 1 female patient)" [OMIM:Premature pubarche (in 1 female patient)]
OMIM: "Premature pubarche (in some patients)" [OMIM:Premature pubarche (in some patients)]
UMLS:C0034013 "Precocious Puberty" [Orphanet:41750]
Is a (Direct Parents):
Orphanet Abnormality of the endocrine system
MedDRA Endocrine abnormalities of puberty
HPO         Early onset of sexual maturation
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the endocrine system(HPO:0000818)
          Puberty and gonadal disorders(HPO:0008373)
             Early onset of sexual maturation(HPO:0100000)
                Precocious puberty(HPO:0000826)
MedDRA:
Endocrine disorders(MedDRA:10014698)
    Endocrine disorders of gonadal function(MedDRA:10014701)
       Endocrine abnormalities of puberty(MedDRA:10014692)
          Precocious puberty(HPO:0000826)
Database Frequency: 42 / 7739
Resource:

All diseases associated with this symptom:

19p13.12 microdeletion syndrome (Orphanet:254346)
Aicardi syndrome (Orphanet:50)
Albright hereditary osteodystrophy (Orphanet:665)
Alexander disease (Orphanet:58)
Alström syndrome (Orphanet:64)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CARPENTER SYNDROME 1 (OMIM:201000)
CORTISONE REDUCTASE DEFICIENCY 2 (OMIM:614662)
Carpenter syndrome (Orphanet:65759)
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (Orphanet:90794)
Cytomegalic congenital adrenal hypoplasia (Orphanet:95702)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
Enchondromatosis (Orphanet:296)
Fibrous dysplasia of bone (Orphanet:249)
Intellectual deficit, X-linked - precocious puberty - obesity (Orphanet:85318)
Kabuki syndrome (Orphanet:2322)
Leprechaunism (Orphanet:508)
Linear nevus sebaceus syndrome (Orphanet:2612)
MICROPHTHALMIA, SYNDROMIC 14 (OMIM:615877)
McCune-Albright syndrome (Orphanet:562)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microduplication Xp11.22-p11.23 syndrome (Orphanet:217377)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Myhre syndrome (Orphanet:2588)
Neurofibromatosis type 1 (Orphanet:636)
Pallister-Hall syndrome (Orphanet:672)
Polyostotic fibrous dysplasia (Orphanet:93276)
Prader-Willi syndrome (Orphanet:739)
Pseudoleprechaunism syndrome, Patterson type (Orphanet:2976)
Rabson-Mendenhall syndrome (Orphanet:769)
Silver-Russell syndrome (Orphanet:813)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Sotos syndrome (Orphanet:821)
Spastic paraplegia - precocious puberty (Orphanet:2826)
Spondyloepimetaphyseal dysplasia, Pakistani type (Orphanet:93282)
TUBEROUS SCLEROSIS 1 (OMIM:191100)
TUBEROUS SCLEROSIS 2 (OMIM:613254)
Testotoxicosis (Orphanet:3000)
Tuberous sclerosis (Orphanet:805)
Williams syndrome (Orphanet:904)
Wolf-Hirschhorn syndrome (Orphanet:280)