Gynecomastia
Symptom Information:
Symptom ID: | HPO:0000771 | ||||||||||||||
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 breast(HPO:0000769) Gynecomastia(HPO:0000771) MedDRA: Reproductive system and breast disorders(MedDRA:10038604) Breast disorders(MedDRA:10006232) Breast disorders NEC(MedDRA:10040675) Gynecomastia(HPO:0000771) |
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Database Frequency: | 53 / 7739 | ||||||||||||||
Resource: |
All diseases associated with this symptom:
2p15p16.1 microdeletion syndrome | (Orphanet:261349) |
46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency | (Orphanet:752) |
48,XXXY syndrome | (Orphanet:96263) |
48,XXYY syndrome | (Orphanet:10) |
49,XXXXY syndrome | (Orphanet:96264) |
ANDROGEN INSENSITIVITY SYNDROME | (OMIM:300068) |
ANE syndrome | (Orphanet:157954) |
Albright hereditary osteodystrophy | (Orphanet:665) |
Alström syndrome | (Orphanet:64) |
Aromatase excess syndrome | (Orphanet:178345) |
Borjeson-Forssman-Lehmann syndrome | (Orphanet:127) |
COWDEN SYNDROME 5 | (OMIM:615108) |
COWDEN SYNDROME 6 | (OMIM:615109) |
Cabezas syndrome | (Orphanet:85293) |
Carney complex | (Orphanet:1359) |
Castleman disease | (Orphanet:160) |
Cerebellar ataxia - hypogonadism | (Orphanet:1173) |
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency | (Orphanet:90794) |
Colobomatous microphthalmia-obesity-hypogenitalism-intellectual disability syndrome | (Orphanet:363741) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency | (Orphanet:90793) |
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome | (Orphanet:306504) |
Cowden syndrome | (Orphanet:201) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
GYNECOMASTIA, FAMILIAL | (OMIM:306500) |
Gorlin syndrome | (Orphanet:377) |
HYPOGONADISM, MALE | (OMIM:307300) |
HYPOGONADISM, MALEHYPOGONADISM AND TESTICULAR ATROPHY, INCLUDED | (OMIM:241100) |
HYPOGONADOTROPIC HYPOGONADISM 1 WITH OR WITHOUT ANOSMIA | (OMIM:308700) |
HYPOGONADOTROPIC HYPOGONADISM 23 WITHOUT ANOSMIA | (OMIM:228300) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Hypoinsulinemic hypoglycemia and body hemihypertrophy | (Orphanet:293964) |
Hyposmia - nasal and ocular hypoplasia - hypogonadotropic hypogonadism | (Orphanet:2250) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA | (OMIM:308750) |
Kallmann syndrome | (Orphanet:478) |
Kennedy disease | (Orphanet:481) |
Leprechaunism | (Orphanet:508) |
Male hypergonadotropic hypogonadism - intellectual deficit - skeletal anomalies | (Orphanet:2234) |
Mikati-Najjar-Sahli syndrome | (Orphanet:2558) |
Normosmic congenital hypogonadotropic hypogonadism | (Orphanet:432) |
Obesity due to congenital leptin deficiency | (Orphanet:66628) |
POEMS syndrome | (Orphanet:2905) |
PSEUDOHERMAPHRODITISM, INCOMPLETE MALE, TYPE I | (OMIM:312100) |
Pachydermoperiostosis | (Orphanet:2796) |
Partial androgen insensitivity syndrome | (Orphanet:90797) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
Riboflavin transporter deficiency | (Orphanet:97229) |
SPERMATOGENIC FAILURE, X-LINKED, 1 | (OMIM:305700) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Wilson-Turner syndrome | (Orphanet:3459) |
Xq27.3q28 duplication syndrome | (Orphanet:261483) |