Hypoplasia of penis

Symptom Information:

Symptom ID: HPO:0008736
Synonyms:
Underdeveloped penis [HPO:0008736]
Hypoplasia of penis [OMIM:Hypoplasia of penis]
Underdeveloped penis [OMIM:Underdeveloped penis]
Quality:
Cross references:
OMIM: "Hypoplasia of penis" [OMIM:Hypoplasia of penis]
OMIM: "Underdeveloped penis" [OMIM:Underdeveloped penis]
Is a (Direct Parents):
HPO         Abnormality of the penis
HPO         Hypoplastic male external genitalia
HPO         Microphallus
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 male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Hypoplastic male external genitalia(HPO:0000050)
                         Hypoplasia of penis(HPO:0008736)
                      Abnormality of the penis(HPO:0000036)
                         Hypoplasia of penis(HPO:0008736)
                Abnormal external genitalia(HPO:0000811)
                   Abnormality of male external genitalia(HPO:0000032)
                      Hypoplastic male external genitalia(HPO:0000050)
                         Hypoplasia of penis(HPO:0008736)
                      Abnormality of the penis(HPO:0000036)
                         Hypoplasia of penis(HPO:0008736)
                   External genital hypoplasia(HPO:0003241)
                      Hypoplastic male external genitalia(HPO:0000050)
                         Hypoplasia of penis(HPO:0008736)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
48,XXYY syndrome (Orphanet:10)
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
Bardet-Biedl syndrome (Orphanet:110)
DYSMYELINATION WITH JAUNDICE (OMIM:224250)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Wilson-Turner syndrome (Orphanet:3459)