Macroorchidism

Symptom Information:

Symptom ID: HPO:0000053
Synonyms:
Large testicle (finding) [Orphanet:39420]
Large testicle [Orphanet:39420]
Macroorchidism [OMIM:Macroorchidism]
Macroorchidism/macrotestes [Orphanet:39420]
Macroorchidism (described in 1 family) [OMIM:Macroorchidism (described in 1 family)]
Quality:
Cross references:
Orphanet:39420 "Macroorchidism/macrotestes" [Orphanet:39420]
OMIM: "Macroorchidism" [OMIM:Macroorchidism]
OMIM: "Macroorchidism (described in 1 family)" [OMIM:Macroorchidism (described in 1 family)]
UMLS:C1263023 "Macroorchidism" [HPO:0000053]
UMLS:C0455913 "Large testicle" [Orphanet:39420]
Is a (Direct Parents):
HPO         Abnormality of the testis
Orphanet Abnormality of the testis
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 internal genitalia(HPO:0000022)
                      Abnormality of the testis(HPO:0000035)
                         Macroorchidism(HPO:0000053)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of male internal genitalia(HPO:0000022)
                      Abnormality of the testis(HPO:0000035)
                         Macroorchidism(HPO:0000053)
MedDRA:
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

17q11.2 microduplication syndrome (Orphanet:139474)
Aspartylglucosaminuria (Orphanet:93)
Atkin-Flaitz syndrome (Orphanet:1193)
CLARK-BARAITSER SYNDROME (OMIM:300602)
Fragile X syndrome (Orphanet:908)
Intellectual deficit, X-linked - macrocephaly - macro-orchidism (Orphanet:85320)
Intellectual deficit, X-linked - psychosis - macroorchidism (Orphanet:3077)
Intellectual deficit, X-linked, Shashi type (Orphanet:85286)
Intellectual deficit, X-linked, Turner type (Orphanet:85328)
MENTAL RETARDATION, X-LINKED 14 (OMIM:300062)
McCune-Albright syndrome (Orphanet:562)
Megalencephaly (Orphanet:2477)
PROLACTIN DEFICIENCY WITH OBESITY AND ENLARGED TESTES (OMIM:264120)
Proteus syndrome (Orphanet:744)
Testotoxicosis (Orphanet:3000)
Trisomy 20p (Orphanet:261318)
X-linked intellectual deficit with marfanoid habitus (Orphanet:776)
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome (Orphanet:324410)