Supernumerary nipple

Symptom Information:

Symptom ID: HPO:0002558
Synonyms:
Accessory nipple [HPO:0002558]
Accessory nipples [HPO:0002558]
Supernumerary nipple [HPO:0002558]
Supernumerary nipple [Orphanet:15400]
Accessory nipple (disorder) [Orphanet:15400]
Accessory nipple [Orphanet:15400]
Accessory nipple [OMIM:Accessory nipple]
Accessory nipples [OMIM:Accessory nipples]
Supernumerary nipple [OMIM:Supernumerary nipple]
Supernumerary nipples [OMIM:Supernumerary nipples]
Supernumerary nipples/polythelia [Orphanet:15400]
Supernumerary nipple [MedDRA:10042571]
Nipple supernumerary [MedDRA:10042571]
Supernumerary nipples (polythelia) [OMIM:Supernumerary nipples (polythelia)]
Quality:
Cross references:
Orphanet:15400 "Supernumerary nipples/polythelia" [Orphanet:15400]
OMIM: "Accessory nipple" [OMIM:Accessory nipple]
OMIM: "Accessory nipples" [OMIM:Accessory nipples]
OMIM: "Supernumerary nipple" [OMIM:Supernumerary nipple]
OMIM: "Supernumerary nipples" [OMIM:Supernumerary nipples]
OMIM: "Supernumerary nipples (polythelia)" [OMIM:Supernumerary nipples (polythelia)]
UMLS:C0266011 "Accessory nipple" [Orphanet:15400]
Is a (Direct Parents):
HPO         Abnormality of the nipple
MedDRA Skin and subcutaneous malformations and anomalies NEC
Orphanet Abnormality of the thorax
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the breast(HPO:0000769)
          Abnormality of the nipple(HPO:0004404)
             Supernumerary nipple(HPO:0002558)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Skin and subcutaneous malformations and anomalies NEC(MedDRA:10040889)
          Supernumerary nipple(HPO:0002558)
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
2q37 microdeletion syndrome (Orphanet:1001)
3MC SYNDROME 1 (OMIM:257920)
ADAMS-OLIVER SYNDROME 1 (OMIM:100300)
Adams-Oliver syndrome (Orphanet:974)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Becker nevus syndrome (Orphanet:64755)
Beckwith-Wiedemann syndrome due to CDKN1C mutation (Orphanet:231120)
Blepharophimosis-intellectual deficit syndrome, Verloes type (Orphanet:293725)
Bohring-Opitz syndrome (Orphanet:97297)
Branchio-oculo-facial syndrome (Orphanet:1297)
CARPENTER SYNDROME 2 (OMIM:614976)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cerebellar ataxia - hypogonadism (Orphanet:1173)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Char syndrome (Orphanet:46627)
Choroidal atrophy - alopecia (Orphanet:1433)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Dysmorphism - conductive hearing loss - heart defect (Orphanet:289553)
Ectodermal dysplasia - intellectual deficit - central nervous system malformation (Orphanet:1812)
Familial supernumerary nipples (Orphanet:2456)
Focal dermal hypoplasia (Orphanet:2092)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hypertrichosis (Orphanet:79365)
Incontinentia pigmenti (Orphanet:464)
Intellectual deficit - athetosis - microphthalmia (Orphanet:1236)
Intellectual deficit - microcephaly - phalangeal - facial abnormalities (Orphanet:3067)
Kleefstra syndrome (Orphanet:261494)
Microcephaly - intellectual deficit - phalangeal and neurological anomalies (Orphanet:137658)
Microcephaly - seizures - intellectual deficit - heart disease (Orphanet:2519)
Mowat-Wilson syndrome (Orphanet:2152)
Oliver syndrome (Orphanet:2920)
Postaxial acrofacial dysostosis (Orphanet:246)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Tetrasomy 12p (Orphanet:884)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Trisomy 12p (Orphanet:1699)