Clitoromegaly
Symptom Information:
Symptom ID: | HPO:0000057 | ||||||||||
Synonyms: |
|
||||||||||
Quality: | |||||||||||
Cross references: |
|
||||||||||
Is a (Direct Parents): |
|
||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the genitourinary system(HPO:0000119) Abnormality of the genital system(HPO:0000078) Abnormal genital system morphology(HPO:0012243) Abnormality of the female genitalia(HPO:0010460) Abnormality of female external genitalia(HPO:0000055) Abnormality of the clitoris(HPO:0000056) Clitoromegaly(HPO:0000057) Abnormal external genitalia(HPO:0000811) Abnormality of female external genitalia(HPO:0000055) Abnormality of the clitoris(HPO:0000056) Clitoromegaly(HPO:0000057) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Vulvovaginal disorders (excl infections and inflammations)(MedDRA:10047789) Vulvovaginal signs and symptoms(MedDRA:10047792) Clitoromegaly(HPO:0000057) |
||||||||||
Database Frequency: | 30 / 7739 | ||||||||||
Resource: |
All diseases associated with this symptom:
46,XX disorder of sex development - skeletal anomalies | (Orphanet:2975) |
46,XY SEX REVERSAL 6 | (OMIM:613762) |
AICA-ribosiduria | (Orphanet:250977) |
ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS | (OMIM:201750) |
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 | (OMIM:170995) |
BOWEN SYNDROME OF MULTIPLE MALFORMATIONS | (OMIM:211200) |
C syndrome | (Orphanet:1308) |
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency | (Orphanet:90795) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
FGFR2-related bent bone dysplasia | (Orphanet:313855) |
Fraser syndrome | (Orphanet:2052) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
LEIOMYOMA OF VULVA AND ESOPHAGUS | (OMIM:150700) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leprechaunism | (Orphanet:508) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
MEIER-GORLIN SYNDROME 2 | (OMIM:613800) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) | (OMIM:214110) |
PEROXISOME BIOGENESIS DISORDER 5A (ZELLWEGER) | (OMIM:614866) |
ROBERTS SYNDROME | (OMIM:268300) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Roberts syndrome | (Orphanet:3103) |
SECKEL SYNDROME 1 | (OMIM:210600) |
Seckel syndrome | (Orphanet:808) |
X-linked diffuse leiomyomatosis - Alport syndrome | (Orphanet:1018) |
Zellweger syndrome | (Orphanet:912) |