Bilateral cryptorchidism
Symptom Information:
Symptom ID: | HPO:0008689 | ||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) 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) Abnormal external genitalia(HPO:0000811) Abnormality of male external genitalia(HPO:0000032) 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) |
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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) |