Hypoplastic nipples
Symptom Information:
Symptom ID: | HPO:0002557 | ||||||||||
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) Abnormality of the nipple(HPO:0004404) Aplasia/Hypoplasia of the nipples(HPO:0006709) Hypoplastic nipples(HPO:0002557) MedDRA: |
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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) |