Abnormality of the nipple
Symptom Information:
| Symptom ID: | HPO:0004404 | ||||
| Synonyms: |
|
||||
| Quality: | |||||
| Cross references: |
|
||||
| Is a (Direct Parents): |
|
||||
| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the breast(HPO:0000769) Abnormality of the nipple(HPO:0004404) MedDRA: |
||||
| Database Frequency: | 54 / 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) |
| 3q13 microdeletion syndrome | (Orphanet:1621) |
| 8q22.1 microdeletion syndrome | (Orphanet:178303) |
| AREDYLD syndrome | (Orphanet:1133) |
| Bird headed-dwarfism, Montreal type | (Orphanet:2617) |
| Bohring-Opitz syndrome | (Orphanet:97297) |
| Brachyolmia, Maroteaux type | (Orphanet:93302) |
| Braddock syndrome | (Orphanet:52047) |
| Brain malformation - congenital heart disease - postaxial polydactyly | (Orphanet:75389) |
| CHARGE syndrome | (Orphanet:138) |
| Cavernous hemangiomas of face - supraumbilical midline raphe | (Orphanet:2124) |
| Congenital disorder of glycosylation | (Orphanet:137) |
| Congenital muscular dystrophy - infantile cataract - hypogonadism | (Orphanet:1875) |
| Craniosynostosis - hydrocephalus - Chiari I malformation - radioulnar synostosis | (Orphanet:171839) |
| Deafness - intellectual deficit, Martin-Probst type | (Orphanet:85321) |
| Disorder of sex development - intellectual deficit | (Orphanet:2983) |
| Distal monosomy 7q36 | (Orphanet:1636) |
| Distal monosomy 9p | (Orphanet:1642) |
| Distal trisomy 6p | (Orphanet:1745) |
| Fetal hydantoin syndrome | (Orphanet:1912) |
| Fraser syndrome | (Orphanet:2052) |
| Fryns syndrome | (Orphanet:2059) |
| Growth delay due to insulin-like growth factor I resistance | (Orphanet:73273) |
| Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
| Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
| Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
| Kousseff syndrome | (Orphanet:2351) |
| Malignant hyperthermia - arthrogryposis - torticollis | (Orphanet:2215) |
| Microcephaly - cardiac defect - lung malsegmentation | (Orphanet:2516) |
| Monosomy 18p | (Orphanet:1598) |
| Monosomy 9p | (Orphanet:261112) |
| Non-distal trisomy 13q | (Orphanet:1702) |
| Noonan syndrome | (Orphanet:648) |
| Orofaciodigital syndrome type 3 | (Orphanet:2752) |
| Parana hard-skin syndrome | (Orphanet:2812) |
| Penoscrotal transposition | (Orphanet:2842) |
| Peters-plus syndrome | (Orphanet:709) |
| Prominent glabella - microcephaly - hypogenitalism | (Orphanet:2083) |
| Pseudoprogeria syndrome | (Orphanet:2985) |
| Ring chromosome 10 | (Orphanet:1438) |
| SCARF syndrome | (Orphanet:3134) |
| Short stature - heart defect - craniofacial anomalies | (Orphanet:1088) |
| Smith-Lemli-Opitz syndrome | (Orphanet:818) |
| Split hand - urinary anomalies - spina bifida | (Orphanet:2437) |
| Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
| Trisomy 1q | (Orphanet:261344) |
| Trisomy 20p | (Orphanet:261318) |
| Trisomy 4p | (Orphanet:1738) |
| Trisomy 9p | (Orphanet:236) |
| Turner syndrome | (Orphanet:881) |
| X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |
| Zlotogora-Ogur syndrome | (Orphanet:3253) |