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380 Possible Causes for Calvarial Hyperostosis

  • Weismann Netter Syndrome

    hyperostosis and delayed eruption of permanent teeth.[orpha.net] Hyperostosis 31 1670 c MND002 Mandibuloacral Dysplasia with Type B Lipodystrophy 31 1671 ORB009 Orbit Lymphoma 31 1672 UND007 Undifferentiated Connective Tissue Disease 30[malacards.org] […] scoliosis with marked lumbar lordosis, horizontal sacrum and square iliac wings and/or, less frequently, vertebral malformations, abnormal shape of the clavicles and ribs, calvarial[orpha.net]

  • Craniorhiny

    hyperostosis Camptodactyly syndrome Guadalajara type 2 Cerebrofrontofacial Syndrome Cerebrooculofacioskeletal Syndrome 2 Cerebrooculofacioskeletal Syndrome 4 Cerebrooculonasal[ctdbase.org] Hyperostosis Camptodactyly Joint Contractures and Facial Skeletal Dysplasia Camptodactyly Syndrome Guadalajara Type 2 Cenani-Lenz syndactyly syndrome Cerebrooculofacioskeletal[rgd.mcw.edu] Hyperostosis Camptodactyly Syndrome Guadalajara Type 2 Cerebrooculofacioskeletal Syndrome 2 Cerebrooculofacioskeletal Syndrome 4 Cerebrooculonasal Syndrome CHITAYAT SYNDROME[rgd.mcw.edu]

  • Lenz-Majewski Syndrome

    Skeletal changes included calvarial hyperostosis, sclerosis of the skull base, an enlarged, sclerotic mandible, broad clavicles and ribs, and diaphyseal undermodeling of the[ncbi.nlm.nih.gov] hyperostosis Abnormality of immune system physiology Malignant hyperthermia Abnormal eyebrow morphology Abnormality of the ureter Sprengel anomaly Increased number of teeth[mendelian.co] […] atresia Thin skin Macroglossia Thick vermilion border Bifid uvula High, narrow palate Delayed eruption of teeth Joint hyperflexibility Abnormality of the penis Broad clavicles Calvarial[mendelian.co]

  • Acrodysostosis

    hyperostosis Overgrowth of skullcap 0004490 Cone-shaped epiphyses of the phalanges of the hand Cone-shaped end part of finger bones 0010230 Congenital onset Symptoms present[rarediseases.info.nih.gov] […] nasal tip Increased width of tip of nose Nasal tip, broad Nasal tip, wide Wide tip of nose [ more ] 0000455 Broad palm Broad hand Broad hands Wide palm [ more ] 0001169 Calvarial[rarediseases.info.nih.gov]

  • Entrapment Neuropathy

    This congenital form of anemia caused hyperplasia of the bone marrow as well as hyperostosis of the entire calvarial bone, which in turn led to optic canal stenosis.[ncbi.nlm.nih.gov]

  • Congenital Cortical Hyperostoses

    (Dorland, 27th ed) Calvarial Hyperostosis campomelic dysplasia Camurati-Engelmann disease Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal Cartilage Hair Hypoplasia[rgd.mcw.edu] This congenital form of anemia caused hyperplasia of the bone marrow as well as hyperostosis of the entire calvarial bone, which in turn led to optic canal stenosis.[thejns.org] Other possible associations include neurofibromatosis type 1, tuberous sclerosis, infantile cortical hyperostosis, Gardner syndrome, and fibrous dysplasia.[rrnursingschool.biz]

  • Non-Syndromic Ocular Stickler Syndrome Type 1 

    hyperostosis (EPIDACH) [MIM: 612714 ] COX6B1 P14854 non-pleiotropic Mitochondrial complex IV deficiency (MT-C4D) [MIM: 220110 ] CPN1 P15169 non-pleiotropic Carboxypeptidase[sbg.bio.ic.ac.uk] […] oxidase deficiency 2 (CEMCOX2) [MIM: 615119 ] Leigh syndrome (LS) [MIM: 256000 ] COX4I2 Q96KJ9 non-pleiotropic Exocrine pancreatic insufficiency dyserythropoietic anemia and calvarial[sbg.bio.ic.ac.uk]

  • Carpotarsal Osteochondromatosis

    hyperostosis, Camera Marugo Cohen syndrome, Campomelia Cumming type, Campomelic dysplasia, Camptobrachydactyly, Camptocormism, Camptodactyly arthropathy coxa vara pericarditis[yumpu.com] hyperostosis X-linked dominant chondrodysplasia punctata X-linked hypophosphatemia X-linked osteoporosis with fractures X-linked skeletal dysplasia-intellectual disability[se-atlas.de] […] multiple, Caffey disease, CAHMR syndrome, Calabro syndrome, Calcifying Epi the lial Odontogenic Tumor, Calciphylaxis, California encephalitis, Calloso-genital dysplasia, Calvarial[yumpu.com]

  • Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome

    hyperostosis Exostoses, multiple Fanconi anemia, complementation group Q Feingold syndrome Fibrochondrogenesis Fibrodysplasia ossificans progressiva Fibrosis of extraocular[qlinics.com] hyperostosis Combined deficiency of vitamin K-dependent clotting factors (VKCFD) Adult i phenotype [PATH:hsa00601] Paroxysmal nocturnal hemoglobinuria (PNH) Fletcher factor[csirnotes.com] DSG1 Erythrokeratodermia variabilis et progressive GJB3 Erythrokeratodermia variabilis et progressive GJB4 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial[centogene.com]

  • Dilated Cardiomyopathy Type 2B

    1q44 Mitochondrial complex IV deficiency 220110 614698 Mitochondrial; Autosomal recessive COX4I2 20q11.21 Exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial[mnglabs.com] hyperostosis 612714 607976 Autosomal recessive COX6A1 12q24.31 Charcot-Marie-Tooth disease, recessive intermediate D 616039 602072 Autosomal recessive COX6B1 19q13.12 Mitochondrial[mnglabs.com]

Further symptoms