Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Coarse_facial_features> ?p ?o }
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- Coarse_facial_features abstract "Coarse facial features or "'coarse facies"' describes a constellation of facial features that are present in many inborn errors of metabolism.Features include: large, bulging head prominent scalp veins "saddle-like, flat bridged nose with broad, fleshy tip" large lips and tongue small, widely spaced and/or malformed teeth hypertrophic alveolar ridges and/or gumsHeads tend to be longer than normal from front to back, with a bulging forehead. This is because of the earlier than normal or premature fusion of skull bones in an affected individual.".
- Coarse_facial_features wikiPageExternalLink mps_pt_symptom_coarse_facial_features.asp.
- Coarse_facial_features wikiPageExternalLink www.wrongdiagnosis.com.
- Coarse_facial_features wikiPageID "20935954".
- Coarse_facial_features wikiPageLength "3707".
- Coarse_facial_features wikiPageOutDegree "60".
- Coarse_facial_features wikiPageRevisionID "602308550".
- Coarse_facial_features wikiPageWikiLink Acromegaly.
- Coarse_facial_features wikiPageWikiLink Alpha-mannosidosis_type_II.
- Coarse_facial_features wikiPageWikiLink Aspartylglucosaminuria.
- Coarse_facial_features wikiPageWikiLink Aspartylglycosaminuria.
- Coarse_facial_features wikiPageWikiLink Battaglia_Neri_syndrome.
- Coarse_facial_features wikiPageWikiLink Borjeson_Syndrome.
- Coarse_facial_features wikiPageWikiLink Category:Facial_features.
- Coarse_facial_features wikiPageWikiLink Chromosome_6q_deletion_syndrome.
- Coarse_facial_features wikiPageWikiLink Coarse_face_-_hypotonia_-_constipation.
- Coarse_facial_features wikiPageWikiLink Congenital_hypothyroidism.
- Coarse_facial_features wikiPageWikiLink Dandy-Walker_malformation_(with_mental_retardation_basal_ganglia_disease_and_seizures).
- Coarse_facial_features wikiPageWikiLink Dyggve-Melchior-Clausen_Syndrome.
- Coarse_facial_features wikiPageWikiLink Facies_(medical).
- Coarse_facial_features wikiPageWikiLink Fucosidosis.
- Coarse_facial_features wikiPageWikiLink Fucosidosis_type_1.
- Coarse_facial_features wikiPageWikiLink Fucosidosis_type_II.
- Coarse_facial_features wikiPageWikiLink GM1_gangliosidoses.
- Coarse_facial_features wikiPageWikiLink GM1_gangliosidosis.
- Coarse_facial_features wikiPageWikiLink Gangliosidosis_GM1_(type_3).
- Coarse_facial_features wikiPageWikiLink Gangliosidosis_generalized_GM1_(type_1).
- Coarse_facial_features wikiPageWikiLink Goldberg_syndrome.
- Coarse_facial_features wikiPageWikiLink Hunter_syndrome.
- Coarse_facial_features wikiPageWikiLink Hyde-Forster-Mccarthy-Berry_syndrome.
- Coarse_facial_features wikiPageWikiLink Hyper_IgE.
- Coarse_facial_features wikiPageWikiLink Hyperimmunoglobulin_E_syndrome.
- Coarse_facial_features wikiPageWikiLink Hypomelanosis_of_Ito.
- Coarse_facial_features wikiPageWikiLink I-cell_disease.
- Coarse_facial_features wikiPageWikiLink I_cell_disease.
- Coarse_facial_features wikiPageWikiLink Immunodeficiency_due_to_defect_in_MAPBP-interacting_protein.
- Coarse_facial_features wikiPageWikiLink Inborn_error_of_metabolism.
- Coarse_facial_features wikiPageWikiLink Inborn_errors_of_metabolism.
- Coarse_facial_features wikiPageWikiLink Incontinentia_pigmenti_achromians.
- Coarse_facial_features wikiPageWikiLink Infantile_free_sialic_acid_storage_disease.
- Coarse_facial_features wikiPageWikiLink Infantile_sialic_acid_storage_disorder.
- Coarse_facial_features wikiPageWikiLink Job_syndrome.
- Coarse_facial_features wikiPageWikiLink MPS_3_C.
- Coarse_facial_features wikiPageWikiLink MPS_3_D.
- Coarse_facial_features wikiPageWikiLink Mannosidosis_(alpha_B_lysosomal).
- Coarse_facial_features wikiPageWikiLink Maroteaux–Lamy_syndrome.
- Coarse_facial_features wikiPageWikiLink McCune-Albright_Syndrome.
- Coarse_facial_features wikiPageWikiLink McCune–Albright_syndrome.
- Coarse_facial_features wikiPageWikiLink Mental_retardation_(X-linked_-_epilepsy_-_progressive_joint_contractures_-_typical_face).
- Coarse_facial_features wikiPageWikiLink Mental_retardation_(X-linked_Raynaud_type).
- Coarse_facial_features wikiPageWikiLink Mieschers_syndrome.
- Coarse_facial_features wikiPageWikiLink Morquio_syndrome.
- Coarse_facial_features wikiPageWikiLink Morquio_syndrome_type_A.
- Coarse_facial_features wikiPageWikiLink Morquio_syndrome_type_B.
- Coarse_facial_features wikiPageWikiLink Mucolipidosis_III.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_2_Hunter_syndrome-_mild_form.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_2_Hunter_syndrome-_severe_form.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_3.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_6.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_7_Sly_syndrome.
- Coarse_facial_features wikiPageWikiLink Scheie_syndrome.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_I_Hurler_syndrome.
- Coarse_facial_features wikiPageWikiLink Mucopolysaccharidosis_type_I_Scheie_syndrome.
- Coarse_facial_features wikiPageWikiLink Multiple_endocrine_abnormalities_-_adenylyl_cyclase_dysfunction.
- Coarse_facial_features wikiPageWikiLink Multiple_endocrine_neoplasia_type_2b.
- Coarse_facial_features wikiPageWikiLink Neuraminidase_deficiency_(type_II_juvenile_form).
- Coarse_facial_features wikiPageWikiLink Nodulosis-arthropathy-osteolysis_syndrome.
- Coarse_facial_features wikiPageWikiLink Nodulosis–arthropathy–osteolysis_syndrome.
- Coarse_facial_features wikiPageWikiLink Nonkeratan-sulfate-excreting_Morquio_syndrome.
- Coarse_facial_features wikiPageWikiLink Pituitary_tumors_(adult).
- Coarse_facial_features wikiPageWikiLink Pseudo-Hurler_polydystrophy.
- Coarse_facial_features wikiPageWikiLink Sialidosis_type_II_(congenital).
- Coarse_facial_features wikiPageWikiLink Sialidosis_type_II_(infantile).
- Coarse_facial_features wikiPageWikiLink Sialuria.
- Coarse_facial_features wikiPageWikiLink Simpson-Golabi-Behmel_syndrome.
- Coarse_facial_features wikiPageWikiLink Simpson-Golabi-Behmel_syndrome_-_type_1_(SGBS1).
- Coarse_facial_features wikiPageWikiLink Simpson–Golabi–Behmel_syndrome.
- Coarse_facial_features wikiPageWikiLink Skeletal_dysplasia_-_coarse_facies_-_mental_retardation.
- Coarse_facial_features wikiPageWikiLink Spondyloepimetaphyseal_dysplasia_(genevieve_type).
- Coarse_facial_features wikiPageWikiLink Sulfatidosis_juvenile_(Austin_type).
- Coarse_facial_features wikiPageWikiLink Winchester_syndrome.
- Coarse_facial_features wikiPageWikiLinkText "Coarse facial features".
- Coarse_facial_features wikiPageWikiLinkText "coarse facial appearance".
- Coarse_facial_features wikiPageWikiLinkText "coarse facial features".
- Coarse_facial_features hasPhotoCollection Coarse_facial_features.
- Coarse_facial_features wikiPageUsesTemplate Template:Reflist.
- Coarse_facial_features wikiPageUsesTemplate Template:Symptom-stub.
- Coarse_facial_features subject Category:Facial_features.
- Coarse_facial_features type Feature.
- Coarse_facial_features comment "Coarse facial features or "'coarse facies"' describes a constellation of facial features that are present in many inborn errors of metabolism.Features include: large, bulging head prominent scalp veins "saddle-like, flat bridged nose with broad, fleshy tip" large lips and tongue small, widely spaced and/or malformed teeth hypertrophic alveolar ridges and/or gumsHeads tend to be longer than normal from front to back, with a bulging forehead.".
- Coarse_facial_features label "Coarse facial features".
- Coarse_facial_features sameAs m.05b0h2y.
- Coarse_facial_features sameAs Q5138061.
- Coarse_facial_features sameAs Q5138061.
- Coarse_facial_features wasDerivedFrom Coarse_facial_features?oldid=602308550.
- Coarse_facial_features isPrimaryTopicOf Coarse_facial_features.