Clitoral hypoplasia

Symptom Information:

Symptom ID: HPO:0000060
Synonyms:
Hypoplastic clitoris [HPO:0000060]
Small clitoris [HPO:0000060]
Clitoris hypoplasia [Orphanet:39120]
Clitoral hypoplasia [OMIM:Clitoral hypoplasia]
Hypoplastic clitoris [OMIM:Hypoplastic clitoris]
Small clitoris [OMIM:Small clitoris]
Clitoris/labia majora/labia minora/female external genitalia hypoplasia [Orphanet:39120]
Small clitoris (46%) [OMIM:Small clitoris (46%)]
Small clitoris (80%) [OMIM:Small clitoris (80%)]
Female external genitalia hypoplasia [Orphanet:39120]
Quality:
Cross references:
Orphanet:39120 "Clitoris/labia majora/labia minora/female external genitalia hypoplasia" [Orphanet:39120]
OMIM: "Clitoral hypoplasia" [OMIM:Clitoral hypoplasia]
OMIM: "Hypoplastic clitoris" [OMIM:Hypoplastic clitoris]
OMIM: "Small clitoris" [OMIM:Small clitoris]
OMIM: "Small clitoris (46%)" [OMIM:Small clitoris (46%)]
OMIM: "Small clitoris (80%)" [OMIM:Small clitoris (80%)]
Is a (Direct Parents):
Orphanet Structural anomalies of the genital system
Orphanet Hypoplastic labia majora
HPO         Abnormality of the clitoris
HPO         External genital hypoplasia
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)
                   External genital hypoplasia(HPO:0003241)
                      Clitoral hypoplasia(HPO:0000060)
                   Abnormality of female external genitalia(HPO:0000055)
                      Abnormality of the clitoris(HPO:0000056)
                         Clitoral hypoplasia(HPO:0000060)
                Abnormality of the female genitalia(HPO:0010460)
                   Abnormality of female external genitalia(HPO:0000055)
                      Abnormality of the clitoris(HPO:0000056)
                         Clitoral hypoplasia(HPO:0000060)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Focal dermal hypoplasia (Orphanet:2092)
Jacobsen syndrome (Orphanet:2308)
Peters-plus syndrome (Orphanet:709)
Prader-Willi syndrome (Orphanet:739)
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome (Orphanet:314394)