Bilateral cryptorchidism

Symptom Information:

Symptom ID: HPO:0008689
Synonyms:
Cryptorchidism, bilateral [HPO:0008689]
Cryptorchidism [Orphanet:39380]
Undescended testis (body structure) [Orphanet:39380]
Undescended testicle (disorder) [Orphanet:39380]
Bilateral cryptorchidism [OMIM:Bilateral cryptorchidism]
Cryptorchidism, bilateral [OMIM:Cryptorchidism, bilateral]
Undescended/ectopic testes/cryptorchidia/unfixed testes [Orphanet:39380]
Cryptorchism [Orphanet:39380]
Cryptorchism [MedDRA:10011498]
Maldescended testicle [MedDRA:10011498]
Maldescended testis [MedDRA:10011498]
Testicle maldescended [MedDRA:10011498]
Testicle undescended [MedDRA:10011498]
Undescended testicle [MedDRA:10011498]
Undescended testis [MedDRA:10011498]
Cryptorchidism [MedDRA:10011498]
Ectopic testis [MedDRA:10011498]
Cryptorchidism (1 patient) [OMIM:Cryptorchidism (1 patient)]
Cryptorchidism (67%) [OMIM:Cryptorchidism (67%)]
Cryptorchidism (72%) [OMIM:Cryptorchidism (72%)]
Cryptorchidism (in 1 of 3 siblings) [OMIM:Cryptorchidism (in 1 of 3 siblings)]
Cryptorchidism (in most patients) [OMIM:Cryptorchidism (in most patients)]
Cryptorchidism (in some patients) [OMIM:Cryptorchidism (in some patients)]
Cryptorchidism (rare) [OMIM:Cryptorchidism (rare)]
Cryptorchidism (testes in inguinal canal) [OMIM:Cryptorchidism (testes in inguinal canal)]
Cryptorchidism (uncommon) [OMIM:Cryptorchidism (uncommon)]
Cryptorchidism (unilateral or bilateral) [OMIM:Cryptorchidism (unilateral or bilateral)]
Cryptorchidism, bilateral (in some patients) [OMIM:Cryptorchidism, bilateral (in some patients)]
Ectopic testis [OMIM:Ectopic testis]
Undescended testis (rare) [OMIM:Undescended testis (rare)]
Testicular retraction [MedDRA:10043348]
Retractile testis [Orphanet:39380]
Retractile testis (disorder) [Orphanet:39380]
Ectopic testis [MedDRA:10059170]
Ectopic testis (disorder) [Orphanet:39380]
Ectopic testis [Orphanet:39380]
Quality:
Cross references:
HPO:0000028 "Cryptorchidism" [Orphanet:39380]
Orphanet:39380 "Undescended/ectopic testes/cryptorchidia/unfixed testes" [Orphanet:39380]
OMIM: "Bilateral cryptorchidism" [OMIM:Bilateral cryptorchidism]
OMIM: "Cryptorchidism, bilateral" [OMIM:Cryptorchidism, bilateral]
OMIM: "Cryptorchidism (1 patient)" [OMIM:Cryptorchidism (1 patient)]
OMIM: "Cryptorchidism (67%)" [OMIM:Cryptorchidism (67%)]
OMIM: "Cryptorchidism (72%)" [OMIM:Cryptorchidism (72%)]
OMIM: "Cryptorchidism (in 1 of 3 siblings)" [OMIM:Cryptorchidism (in 1 of 3 siblings)]
OMIM: "Cryptorchidism (in most patients)" [OMIM:Cryptorchidism (in most patients)]
OMIM: "Cryptorchidism (in some patients)" [OMIM:Cryptorchidism (in some patients)]
OMIM: "Cryptorchidism (rare)" [OMIM:Cryptorchidism (rare)]
OMIM: "Cryptorchidism (testes in inguinal canal)" [OMIM:Cryptorchidism (testes in inguinal canal)]
OMIM: "Cryptorchidism (uncommon)" [OMIM:Cryptorchidism (uncommon)]
OMIM: "Cryptorchidism (unilateral or bilateral)" [OMIM:Cryptorchidism (unilateral or bilateral)]
OMIM: "Cryptorchidism, bilateral (in some patients)" [OMIM:Cryptorchidism, bilateral (in some patients)]
OMIM: "Ectopic testis" [OMIM:Ectopic testis]
OMIM: "Undescended testis (rare)" [OMIM:Undescended testis (rare)]
UMLS:C0010417 "Cryptorchidism" [Orphanet:39380]
UMLS:C0520578 "Retractile testis" [Orphanet:39380]
UMLS:C0302889 "Ectopic testis" [Orphanet:39380]
Is a (Direct Parents):
Orphanet Cryptorchidism
HPO         Cryptorchidism
Orphanet Abnormality of the testis
MedDRA Male reproductive tract disorders congenital
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 male external genitalia(HPO:0000032)
                      Cryptorchidism(HPO:0000028)
                         Bilateral cryptorchidism(HPO:0008689)
                Abnormality of the male genitalia(HPO:0010461)
                   Abnormality of male external genitalia(HPO:0000032)
                      Cryptorchidism(HPO:0000028)
                         Bilateral cryptorchidism(HPO:0008689)
                   Abnormality of male internal genitalia(HPO:0000022)
                      Abnormality of the testis(HPO:0000035)
                         Cryptorchidism(HPO:0000028)
                            Bilateral cryptorchidism(HPO:0008689)
                Abnormal internal genitalia(HPO:0000812)
                   Abnormality of male internal genitalia(HPO:0000022)
                      Abnormality of the testis(HPO:0000035)
                         Cryptorchidism(HPO:0000028)
                            Bilateral cryptorchidism(HPO:0008689)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Reproductive tract and breast disorders congenital(MedDRA:10038608)
       Male reproductive tract disorders congenital(MedDRA:10025517)
          Bilateral cryptorchidism(HPO:0008689)
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
3-methylglutaconic aciduria type 4 (Orphanet:67048)
3MC SYNDROME 3 (OMIM:248340)
48,XXYY syndrome (Orphanet:10)
Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Atherosclerosis - deafness - diabetes - epilepsy - nephropathy (Orphanet:1192)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Bardet-Biedl syndrome (Orphanet:110)
Bartsocas-Papas syndrome (Orphanet:1234)
Bloom syndrome (Orphanet:125)
Carney complex (Orphanet:1359)
DPAGT1-CDG (Orphanet:86309)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Distal monosomy 3p (Orphanet:1620)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 (OMIM:601776)
FANCONI ANEMIA, COMPLEMENTATION GROUP P (OMIM:613951)
Floating-Harbor syndrome (Orphanet:2044)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA (OMIM:614858)
Intellectual deficit - cataracts - calcified pinnae - myopathy (Orphanet:3042)
LEOPARD SYNDROME 1 (OMIM:151100)
Leprechaunism (Orphanet:508)
MACS syndrome (Orphanet:217335)
MICROPHTHALMIA, SYNDROMIC 12 (OMIM:615524)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mowat-Wilson syndrome (Orphanet:2152)
Noonan syndrome with multiple lentigines (Orphanet:500)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)
Persistent Müllerian duct syndrome (Orphanet:2856)
Porencephaly-microcephaly-bilateral congenital cataract syndrome (Orphanet:306547)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Steinert myotonic dystrophy (Orphanet:273)
Syndromic microphthalmia type 5 (Orphanet:178364)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Wilson-Turner syndrome (Orphanet:3459)