Clitoromegaly

Symptom Information:

Symptom ID: HPO:0000057
Synonyms:
Clitoral enlargement [HPO:0000057]
Enlarged clitoris [HPO:0000057]
Prominent clitoris [HPO:0000057]
Clitoral enlargement [OMIM:Clitoral enlargement]
Clitoromegaly [OMIM:Clitoromegaly]
Enlarged clitoris [OMIM:Enlarged clitoris]
Prominent clitoris [OMIM:Prominent clitoris]
Clitoris enlarged [OMIM:Clitoris enlarged]
Clitoromegaly (rare) [OMIM:Clitoromegaly (rare)]
Enlarged clitoris [MedDRA:10014838]
Quality:
Cross references:
OMIM: "Clitoral enlargement" [OMIM:Clitoral enlargement]
OMIM: "Clitoromegaly" [OMIM:Clitoromegaly]
OMIM: "Enlarged clitoris" [OMIM:Enlarged clitoris]
OMIM: "Prominent clitoris" [OMIM:Prominent clitoris]
OMIM: "Clitoris enlarged" [OMIM:Clitoris enlarged]
OMIM: "Clitoromegaly (rare)" [OMIM:Clitoromegaly (rare)]
Is a (Direct Parents):
HPO         Abnormality of the clitoris
MedDRA Vulvovaginal signs and symptoms
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)
                Abnormal external genitalia(HPO:0000811)
                   Abnormality of female external genitalia(HPO:0000055)
                      Abnormality of the clitoris(HPO:0000056)
                         Clitoromegaly(HPO:0000057)
                Abnormality of the female genitalia(HPO:0010460)
                   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)