Hypoplastic nipples

Symptom Information:

Symptom ID: HPO:0002557
Synonyms:
Nipple hypoplasia [HPO:0002557]
Small nipples [HPO:0002557]
Nipple hypoplasia [Orphanet:15520]
Hypoplasia of nipple (disorder) [Orphanet:15520]
Hypoplasia of nipple [Orphanet:15520]
Hypoplastic nipples [OMIM:Hypoplastic nipples]
Nipple hypoplasia [OMIM:Nipple hypoplasia]
Small nipples [OMIM:Small nipples]
Hypoplastic/absent nipples [Orphanet:15520]
Hypoplastic-absent nipples [OMIM:Hypoplastic-absent nipples]
Quality:
Cross references:
HPO:0006709 "Aplasia/Hypoplasia of the nipples" [Orphanet:15520]
Orphanet:15520 "Hypoplastic/absent nipples" [Orphanet:15520]
OMIM: "Hypoplastic nipples" [OMIM:Hypoplastic nipples]
OMIM: "Nipple hypoplasia" [OMIM:Nipple hypoplasia]
OMIM: "Small nipples" [OMIM:Small nipples]
OMIM: "Hypoplastic-absent nipples" [OMIM:Hypoplastic-absent nipples]
UMLS:C0432355 "Hypoplasia of nipple" [Orphanet:15520]
Is a (Direct Parents):
Orphanet Abnormality of the thorax
HPO         Aplasia/Hypoplasia of the nipples
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the breast(HPO:0000769)
          Abnormality of the nipple(HPO:0004404)
             Aplasia/Hypoplasia of the nipples(HPO:0006709)
                Hypoplastic nipples(HPO:0002557)
MedDRA:
Database Frequency: 33 / 7739
Resource:

All diseases associated with this symptom:

8q22.1 microdeletion syndrome (Orphanet:178303)
ADULT syndrome (Orphanet:978)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Barber-Say syndrome (Orphanet:1231)
Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion (Orphanet:231130)
CARPENTER SYNDROME 2 (OMIM:614976)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
Cornelia de Lange syndrome (Orphanet:199)
DK1-CDG (Orphanet:91131)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
ECTODERMAL DYSPLASIA WITH ADRENAL CYST (OMIM:129550)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
Focal dermal hypoplasia (Orphanet:2092)
GAPO syndrome (Orphanet:2067)
Incontinentia pigmenti (Orphanet:464)
Johanson-Blizzard syndrome (Orphanet:2315)
Limb-mammary syndrome (Orphanet:69085)
Neonatal hemochromatosis (Orphanet:446)
Oculoosteocutaneous syndrome (Orphanet:2713)
Odontotrichomelic syndrome (Orphanet:2723)
Pachygyria - epilepsy - intellectual deficit - dysmorphism (Orphanet:94084)
Phocomelia, Schinzel type (Orphanet:2879)
SCARF syndrome (Orphanet:3134)
Schinzel-Giedion syndrome (Orphanet:798)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short stature - craniofacial anomalies - genital hypoplasia (Orphanet:2994)
Sialuria (Orphanet:3166)
Ulnar-mammary syndrome (Orphanet:3138)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Zunich-Kaye syndrome (Orphanet:3474)