Gynecomastia

Symptom Information:

Symptom ID: HPO:0000771
Synonyms:
Gynaecomastia [HPO:0000771]
Gynecomastia (disorder) [Orphanet:15480]
Gynecomastia [Orphanet:15480]
Gynecomastia [OMIM:Gynecomastia]
Gynecomastia/breast/mammary gland enlargement/hyperplasia [Orphanet:15480]
Gynaecomastia [Orphanet:15480]
Gynaecomastia [MedDRA:10018800]
Breast enlargement male [MedDRA:10018800]
Breast enlargement male bilateral [MedDRA:10018800]
Enlargement breast male [MedDRA:10018800]
Gynecomastia [MedDRA:10018800]
Gynaecomastia aggravated [MedDRA:10018800]
Gynecomastia aggravated [MedDRA:10018800]
Breast enlargement male unilateral [MedDRA:10018800]
Quality:
Cross references:
Orphanet:15480 "Gynecomastia/breast/mammary gland enlargement/hyperplasia" [Orphanet:15480]
OMIM: "Gynecomastia" [OMIM:Gynecomastia]
UMLS:C0018418 "Gynecomastia" [HPO:0000771]
UMLS:C0018418 "Gynecomastia" [Orphanet:15480]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Abnormality of the breast
MedDRA Breast disorders NEC
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)
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)