Hypoplastic labia minora

Symptom Information:

Symptom ID: HPO:0000064
Synonyms:
Labia minora hypoplasia [Orphanet:39120]
Hypoplastic labia minora [OMIM:Hypoplastic labia minora]
Clitoris/labia majora/labia minora/female external genitalia hypoplasia [Orphanet:39120]
Female external genitalia hypoplasia [Orphanet:39120]
Quality:
Cross references:
Orphanet:39120 "Clitoris/labia majora/labia minora/female external genitalia hypoplasia" [Orphanet:39120]
OMIM: "Hypoplastic labia minora" [OMIM:Hypoplastic labia minora]
Is a (Direct Parents):
HPO         Labial hypoplasia
Orphanet Hypoplastic labia majora
Orphanet Structural anomalies of the genital system
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 labia(HPO:0000058)
                         Labial hypoplasia(HPO:0000066)
                            Hypoplastic labia minora(HPO:0000064)
                Abnormal external genitalia(HPO:0000811)
                   External genital hypoplasia(HPO:0003241)
                      Labial hypoplasia(HPO:0000066)
                         Hypoplastic labia minora(HPO:0000064)
                   Abnormality of female external genitalia(HPO:0000055)
                      Abnormality of the labia(HPO:0000058)
                         Labial hypoplasia(HPO:0000066)
                            Hypoplastic labia minora(HPO:0000064)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
AREDYLD syndrome (Orphanet:1133)
Alström syndrome (Orphanet:64)
Ear-patella-short stature syndrome (Orphanet:2554)
MEIER-GORLIN SYNDROME 1 (OMIM:224690)
Prader-Willi syndrome (Orphanet:739)
Schinzel-Giedion syndrome (Orphanet:798)