Aplasia/Hypoplasia of the nipples

Symptom Information:

Symptom ID: HPO:0006709
Absent/rudimentary nipples [HPO:0006709]
Nipples absent or rudimentary [HPO:0006709]
Nipple hypoplasia [Orphanet:15520]
Absent nipple [Orphanet:15520]
Hypoplasia of nipple (disorder) [Orphanet:15520]
Congenital absence of nipple (disorder) [Orphanet:15520]
Absent nipple (finding) [Orphanet:15520]
Hypoplasia of nipple [Orphanet:15520]
Congenital absent nipple [Orphanet:15520]
Nipples absent or rudimentary [OMIM:Nipples absent or rudimentary]
Hypoplastic/absent nipples [Orphanet:15520]
Absent/rudimentary nipples (athelia/hypothelia) [OMIM:Absent/rudimentary nipples (athelia/hypothelia)]
Hypoplastic-absent nipples [OMIM:Hypoplastic-absent nipples]
Cross references:
HPO:0002557 "Hypoplastic nipples" [Orphanet:15520]
HPO:0002561 "Absent nipples" [Orphanet:15520]
Orphanet:15520 "Hypoplastic/absent nipples" [Orphanet:15520]
OMIM: "Nipples absent or rudimentary" [OMIM:Nipples absent or rudimentary]
OMIM: "Absent/rudimentary nipples (athelia/hypothelia)" [OMIM:Absent/rudimentary nipples (athelia/hypothelia)]
OMIM: "Hypoplastic-absent nipples" [OMIM:Hypoplastic-absent nipples]
UMLS:C0432355 "Hypoplasia of nipple" [Orphanet:15520]
UMLS:C0175755 "Congenital absent nipple" [Orphanet:15520]
UMLS:C0425795 "Absent nipple (finding)" [Orphanet:15520]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Abnormality of the nipple
Orphanet Hypoplastic nipples
Is a (Whole tree): HPO:
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the breast(HPO:0000769)
          Abnormality of the nipple(HPO:0004404)
             Aplasia/Hypoplasia of the nipples(HPO:0006709)
Database Frequency: 28 / 7739

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
ADULT syndrome (Orphanet:978)
Ablepharon macrostomia syndrome (Orphanet:920)
Acro-pectoro-renal dysplasia (Orphanet:956)
Barber-Say syndrome (Orphanet:1231)
Cleft palate - large ears - small head (Orphanet:2013)
Congenital disorder of glycosylation (Orphanet:137)
Cornelia de Lange syndrome (Orphanet:199)
Craniofrontonasal dysplasia (Orphanet:1520)
DK1-CDG (Orphanet:91131)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
EEC syndrome (Orphanet:1896)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Fryns syndrome (Orphanet:2059)
Neonatal hemochromatosis (Orphanet:446)
Odontotrichomelic syndrome (Orphanet:2723)
Poland syndrome (Orphanet:2911)
SCARF syndrome (Orphanet:3134)
Scalp-ear-nipple syndrome (Orphanet:2036)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Tetraamelia - multiple malformations (Orphanet:3301)
Turner syndrome (Orphanet:881)
Ulnar-mammary syndrome (Orphanet:3138)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Yunis-Varon syndrome (Orphanet:3472)
Zunich-Kaye syndrome (Orphanet:3474)