Widely spaced teeth

Symptom Information:

Symptom ID: HPO:0000687
Synonyms:
Multiple diastemata [HPO:0000687]
Wide-spaced teeth [HPO:0000687]
Widely-spaced teeth [HPO:0000687]
Wide-spaced teeth [OMIM:Wide-spaced teeth]
Widely spaced teeth [OMIM:Widely spaced teeth]
Widely-spaced teeth [OMIM:Widely-spaced teeth]
Widely spaced teeth (11 of 21) [OMIM:Widely spaced teeth (11 of 21)]
Quality:
Cross references:
OMIM: "Wide-spaced teeth" [OMIM:Wide-spaced teeth]
OMIM: "Widely spaced teeth" [OMIM:Widely spaced teeth]
OMIM: "Widely-spaced teeth" [OMIM:Widely-spaced teeth]
OMIM: "Widely spaced teeth (11 of 21)" [OMIM:Widely spaced teeth (11 of 21)]
Is a (Direct Parents):
HPO         Misalignment of teeth
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the teeth(HPO:0000164)
                         Misalignment of teeth(HPO:0000692)
                            Widely spaced teeth(HPO:0000687)
MedDRA:
Database Frequency: 40 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
2q23.1 microdeletion syndrome (Orphanet:228402)
Adenylosuccinate lyase deficiency (Orphanet:46)
Alpha-mannosidosis (Orphanet:61)
Angelman syndrome (Orphanet:72)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Autosomal dominant nonsyndromic intellectual deficit (Orphanet:178469)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Brachyolmia-amelogenesis imperfecta syndrome (Orphanet:2899)
CHST3-related skeletal dysplasia (Orphanet:263463)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1 (OMIM:122000)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Coffin-Lowry syndrome (Orphanet:192)
Cornelia de Lange syndrome (Orphanet:199)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
EEM syndrome (Orphanet:1897)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
Koolen-De Vries syndrome (Orphanet:96169)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (Orphanet:300496)
OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS (OMIM:257790)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Pitt-Hopkins syndrome (Orphanet:2896)
Posterior polymorphous corneal dystrophy (Orphanet:98973)
RETINAL DYSTROPHY, JUVENILE CATARACTS, AND SHORT STATURE SYNDROME (OMIM:616108)
Tricho-dento-osseous syndrome (Orphanet:3352)
Zunich-Kaye syndrome (Orphanet:3474)