Early onset of sexual maturation
Symptom Information:
Symptom ID: | HPO:0100000 | ||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||||||||||||
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) MedDRA: Endocrine disorders(MedDRA:10014698) Endocrine disorders of gonadal function(MedDRA:10014701) Endocrine abnormalities of puberty(MedDRA:10014692) Early onset of sexual maturation(HPO:0100000) |
||||||||||||||||||||||||||
Database Frequency: | 9 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
CORTISONE REDUCTASE DEFICIENCY 2 | (OMIM:614662) |
Leprechaunism | (Orphanet:508) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Microduplication Xp11.22-p11.23 syndrome | (Orphanet:217377) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Spondyloepimetaphyseal dysplasia, Pakistani type | (Orphanet:93282) |
Williams syndrome | (Orphanet:904) |