Widely spaced teeth
Symptom Information:
Symptom ID: | HPO:0000687 | |||||||
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 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: |
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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) |