Precocious puberty
Symptom Information:
Symptom ID: | HPO:0000826 | |||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |