SHMARQL

Limb–mammary syndrome

<http://www.wikidata.org/entity/Q6549091>

human disease
rdfs:label
"Limb–mammary syndrome"@en
skos:altLabel
"LIMB-MAMMARY SYNDROME"@en
"LIMB-MAMMARY SYNDROME; LMS"@en
"LMS"@en
schema:description
"human disease"@en
schema:dateModified "2026-10-24T00:31:15+00:00"^^xsd:dateTime
schema:version 2560166514
wikibase:identifiers 14
wikibase:sitelinks 4
wikibase:statements 51
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p:direct-normalized/P486 <http://id.nlm.nih.gov/mesh/C535903>
p:direct-normalized/P5270 <http://purl.obolibrary.org/obo/MONDO_0011334>
p:direct-normalized/P5806 <http://snomed.info/id/721972001>
p:direct-normalized/P6366 <https://makg.org/entity/2777203269>
p:direct-normalized/P665 <http://www.kegg.jp/entry/H00640>
wdt:P11430 "DI-01907"
wdt:P1193 0.000001^^xsd:decimal
wdt:P14914 "D69085"
wdt:P1550 "69085"
wdt:P1995 medical genetics
wdt:P2293 TP63
wdt:P279 ectodermal dysplasia
deficient breast volume or number
rare genetic gynecological and obstetrical diseases
syndrome with limb reduction defects
dysostosis of genetic origin with limb anomaly as a major feature
EEC syndrome and related syndrome
wdt:P2841 congenital onset
neonatal onset
wdt:P2888 <http://www.orpha.net/ORDO/Orphanet_69085>
wdt:P2892 "C1863753"
wdt:P31 type of disease
rare disease
wdt:P4317 "10051"
wdt:P486 "C535903"
wdt:P492 "603543"
wdt:P494 "Q82.4"
wdt:P5270 "MONDO_0011334"
wdt:P557 "32743"
wdt:P5806 "721972001"
wdt:P6366 "2777203269"
wdt:P6532 Hypoplastic nipples
cleft lip
syndactyly
Primary amenorrhea
Toe syndactyly
Chronic irritative conjunctivitis
Submucous cleft soft palate
Bilateral breast hypoplasia
Cleft hard palate
tooth agenesis
psoriasis
hypohidrosis
xeroderma
alopecia
cleft palate
bifid uvula
Dysplastic nail
neurofibromatosis type 6
familial congenital nasolacrimal duct obstruction
melanosis
blepharitis
oligodactyly
wdt:P665 "H00640"
wdt:P7807 "1958986288"
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data from SPARQL profile: Wikidata