Wide intermamillary distance

Symptom Information:

Symptom ID: HPO:0006610
Synonyms:
Wide-spaced nipples [HPO:0006610]
Widely spaced nipples [HPO:0006610]
Widely-spaced nipples [HPO:0006610]
Wide spaced nipples [HPO:0006610]
Wide-spaced nipples [OMIM:Wide-spaced nipples]
Widely spaced nipples [OMIM:Widely spaced nipples]
Widely-spaced nipples [OMIM:Widely-spaced nipples]
Widely spaced nipples (1/4 patients) [OMIM:Widely spaced nipples (1/4 patients)]
Widely spaced nipples (in some patients) [OMIM:Widely spaced nipples (in some patients)]
Widely spaced nipples (male) [OMIM:Widely spaced nipples (male)]
Widely-spaced nipples (1 patient) [OMIM:Widely-spaced nipples (1 patient)]
Quality:
Cross references:
OMIM: "Wide-spaced nipples" [OMIM:Wide-spaced nipples]
OMIM: "Widely spaced nipples" [OMIM:Widely spaced nipples]
OMIM: "Widely-spaced nipples" [OMIM:Widely-spaced nipples]
OMIM: "Widely spaced nipples (1/4 patients)" [OMIM:Widely spaced nipples (1/4 patients)]
OMIM: "Widely spaced nipples (in some patients)" [OMIM:Widely spaced nipples (in some patients)]
OMIM: "Widely spaced nipples (male)" [OMIM:Widely spaced nipples (male)]
OMIM: "Widely-spaced nipples (1 patient)" [OMIM:Widely-spaced nipples (1 patient)]
Is a (Direct Parents):
HPO         Abnormality of the nipple
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the breast(HPO:0000769)
          Abnormality of the nipple(HPO:0004404)
             Wide intermamillary distance(HPO:0006610)
MedDRA:
Database Frequency: 46 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
ADULT syndrome (Orphanet:978)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
Bartsocas-Papas syndrome (Orphanet:1234)
Bohring-Opitz syndrome (Orphanet:97297)
Branchio-oculo-facial syndrome (Orphanet:1297)
CARPENTER SYNDROME 2 (OMIM:614976)
CEREBROOCULOFACIOSKELETAL SYNDROME 1 (OMIM:214150)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
CHST3-related skeletal dysplasia (Orphanet:263463)
COFS syndrome (Orphanet:1466)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Camptodactyly syndrome, Guadalajara type 2 (Orphanet:1326)
Carnitine palmitoyl transferase II deficiency, neonatal form (Orphanet:228308)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Distal monosomy 10q (Orphanet:96148)
ENCEPHALOMYOPATHY, MITOCHONDRIAL, DUE TO VOLTAGE-DEPENDENT ANION CHANNELDEFICIENCY (OMIM:614520)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
FACIOTHORACOGENITAL SYNDROME (OMIM:227320)
Fraser syndrome (Orphanet:2052)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
Hypotonia-cerebral atrophy-hyperglycinemia syndrome (Orphanet:363424)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Intellectual deficit, X-linked, Nascimento type (Orphanet:163956)
Intellectual deficit, X-linked, Snyder type (Orphanet:3063)
Koolen-De Vries syndrome (Orphanet:96169)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 (OMIM:615009)
Macrocephaly - spastic paraplegia - dysmorphism (Orphanet:2429)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Monosomy 9p (Orphanet:261112)
Mucolipidosis type 2 (Orphanet:576)
NOONAN SYNDROME 4 (OMIM:610733)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Peters-plus syndrome (Orphanet:709)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
SCARF syndrome (Orphanet:3134)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Subaortic stenosis - short stature (Orphanet:3191)