Decreased testicular size
Symptom Information:
Symptom ID: | HPO:0008734 | ||||||||||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||||||||||
Is a (Direct Parents): | |||||||||||||||||||||||||||||||||
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) Aplasia/Hypoplasia of the testes(HPO:0010468) Decreased testicular size(HPO:0008734) Abnormality of male external genitalia(HPO:0000032) Hypoplastic male external genitalia(HPO:0000050) Decreased testicular size(HPO:0008734) Abnormal external genitalia(HPO:0000811) Abnormality of male external genitalia(HPO:0000032) Hypoplastic male external genitalia(HPO:0000050) Decreased testicular size(HPO:0008734) External genital hypoplasia(HPO:0003241) Hypoplastic male external genitalia(HPO:0000050) Decreased testicular size(HPO:0008734) Abnormal internal genitalia(HPO:0000812) Abnormality of male internal genitalia(HPO:0000022) Abnormality of the testis(HPO:0000035) Aplasia/Hypoplasia of the testes(HPO:0010468) Decreased testicular size(HPO:0008734) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Testicular and epididymal disorders(MedDRA:10013362) Testicular and epididymal disorders NEC(MedDRA:10043296) Decreased testicular size(HPO:0008734) Congenital, familial and genetic disorders(MedDRA:10010331) Reproductive tract and breast disorders congenital(MedDRA:10038608) Male reproductive tract disorders congenital(MedDRA:10025517) Decreased testicular size(HPO:0008734) |
||||||||||||||||||||||||||||||||
Database Frequency: | 105 / 7739 | ||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
2q32q33 microdeletion syndrome | (Orphanet:251019) |
3-phosphoglycerate dehydrogenase deficiency | (Orphanet:79351) |
3M syndrome | (Orphanet:2616) |
3q13 microdeletion syndrome | (Orphanet:1621) |
46,XX testicular disorder of sex development | (Orphanet:393) |
46,XY complete gonadal dysgenesis | (Orphanet:242) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
Alopecia - intellectual deficit - hypergonadotropic hypogonadism | (Orphanet:1014) |
Alström syndrome | (Orphanet:64) |
Aromatase deficiency | (Orphanet:91) |
Ataxia-telangiectasia | (Orphanet:100) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
BRESEK syndrome | (Orphanet:85284) |
Bangstad syndrome | (Orphanet:1227) |
Bardet-Biedl syndrome | (Orphanet:110) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
Brachydactyly - nystagmus - cerebellar ataxia | (Orphanet:1246) |
Cabezas syndrome | (Orphanet:85293) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Caudal appendage - deafness | (Orphanet:1123) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency | (Orphanet:90795) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Congenital ichthyosis - intellectual deficit - spastic quadriplegia | (Orphanet:352333) |
Congenital muscular dystrophy - infantile cataract - hypogonadism | (Orphanet:1875) |
Crandall syndrome | (Orphanet:202) |
Cryptorchidism - arachnodactyly - intellectual deficit | (Orphanet:1548) |
Diabetic embryopathy | (Orphanet:1926) |
Dilated cardiomyopathy with ataxia | (Orphanet:66634) |
Dyskeratosis congenita | (Orphanet:1775) |
Erythrokeratodermia variabilis | (Orphanet:317) |
Fanconi anemia | (Orphanet:84) |
Gemignani syndrome | (Orphanet:2074) |
Genito-palato-cardiac syndrome | (Orphanet:2075) |
HYPOGONADOTROPIC HYPOGONADISM 11 WITH OR WITHOUT ANOSMIA | (OMIM:614840) |
HYPOGONADOTROPIC HYPOGONADISM 12 WITH OR WITHOUT ANOSMIA | (OMIM:614841) |
HYPOGONADOTROPIC HYPOGONADISM 14 WITH OR WITHOUT ANOSMIA | (OMIM:614858) |
HYPOGONADOTROPIC HYPOGONADISM 15 WITH OR WITHOUT ANOSMIA | (OMIM:614880) |
HYPOGONADOTROPIC HYPOGONADISM 16 WITH OR WITHOUT ANOSMIA | (OMIM:614897) |
HYPOGONADOTROPIC HYPOGONADISM 22 WITH OR WITHOUT ANOSMIA | (OMIM:616030) |
HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA | (OMIM:610628) |
HYPOGONADOTROPIC HYPOGONADISM 7 WITH OR WITHOUT ANOSMIA | (OMIM:146110) |
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA | (OMIM:614837) |
Holmes-Gang syndrome | (Orphanet:93970) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Hypergonadotropic hypogonadism - cataract syndrome | (Orphanet:2410) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Hypogonadotropic hypogonadism - frontoparietal alopecia | (Orphanet:2230) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Intellectual deficit, X-linked - short stature - obesity | (Orphanet:3055) |
Intellectual deficit, X-linked, Abidi type | (Orphanet:85273) |
Intellectual deficit, X-linked, Siderius type | (Orphanet:85287) |
Isolated follicle stimulating hormone deficiency | (Orphanet:52901) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
Kallmann syndrome | (Orphanet:478) |
Kennedy disease | (Orphanet:481) |
MENTAL RETARDATION, X-LINKED 92 | (OMIM:300851) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 13 | (OMIM:615287) |
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY | (OMIM:601347) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Mikati-Najjar-Sahli syndrome | (Orphanet:2558) |
Moebius syndrome | (Orphanet:570) |
Monosomy 18p | (Orphanet:1598) |
Mosaic trisomy 8 | (Orphanet:96061) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Normosmic congenital hypogonadotropic hypogonadism | (Orphanet:432) |
Obesity due to congenital leptin deficiency | (Orphanet:66628) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
PAGOD syndrome | (Orphanet:991) |
PREMATURE OVARIAN FAILURE 10 | (OMIM:612885) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
Pallister-Hall syndrome | (Orphanet:672) |
Primary hypergonadotropic hypogonadism - partial alopecia | (Orphanet:2232) |
Prune belly syndrome | (Orphanet:2970) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Renpenning syndrome | (Orphanet:3242) |
Retinitis pigmentosa | (Orphanet:791) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Retinohepatoendocrinologic syndrome | (Orphanet:3087) |
Say-Barber-Miller syndrome | (Orphanet:3132) |
Schwartz-Jampel syndrome | (Orphanet:800) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
Steinert myotonic dystrophy | (Orphanet:273) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
TEMPLE SYNDROME | (OMIM:616222) |
TESTES, RUDIMENTARY | (OMIM:273150) |
THREE M SYNDROME 1 | (OMIM:273750) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Testicular regression syndrome | (Orphanet:983) |
Testotoxicosis | (Orphanet:3000) |
WARBURG MICRO SYNDROME 3 | (OMIM:614222) |
WARBURG MICRO SYNDROME 4 | (OMIM:615663) |
Werner syndrome | (Orphanet:902) |
Wilson-Turner syndrome | (Orphanet:3459) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
X-linked lissencephaly with abnormal genitalia | (Orphanet:452) |
Xeroderma pigmentosum | (Orphanet:910) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |