MCID: HYP364
MIFTS: 29
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Hyperostosis Frontalis Interna
Categories:
Bone diseases, Fetal diseases, Metabolic diseases, Rare diseases
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MalaCards integrated aliases for Hyperostosis Frontalis Interna:
Characteristics:Orphanet epidemiological data:58
morgagni-stewart-morel syndrome
Inheritance: Autosomal dominant,X-linked recessive; Age of onset: Adult; HPO:31Classifications:
MalaCards categories:
Global: Rare diseases Fetal diseases Metabolic diseases Anatomical: Bone diseases
ICD10:
33
Orphanet: 58
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GARD :
20
Morgagni-Stewart-Morel (MSM) syndrome is a disorder characterized by thickening of the frontal bone of the skull (hyperostosis frontalis interna), as well as obesity and excessive hair growth (hypertrichosis). Other signs and symptoms may include seizures, headaches, diabetes insipidus, and sex gland disturbances. The cause of Morgagni-Stewart-Morel syndrome is not fully understood. Some instances of dominant inheritance have been reported, but whether it is autosomal dominant or X-linked dominant is not known. Treatment may include medication for headaches and seizures and surgery to remove the excessive bone of the skull.
MalaCards based summary : Hyperostosis Frontalis Interna, also known as morgagni-stewart-morel syndrome, is related to hyperostosis and acromegaly. Affiliated tissues include bone, brain and eye, and related phenotypes are diabetes mellitus and obesity Wikipedia : 74 Hyperostosis frontalis interna is a common, benign thickening of the inner side of the frontal bone of... more...
More information from OMIM:
144800
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Human phenotypes related to Hyperostosis Frontalis Interna:31 (show all 8)
Symptoms via clinical synopsis from OMIM®:57 (Updated 05-Mar-2021)Clinical features from OMIM®:144800 (Updated 05-Mar-2021) |
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MalaCards organs/tissues related to Hyperostosis Frontalis Interna:40
Bone,
Brain,
Eye,
Cortex,
Breast,
Uterus
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Articles related to Hyperostosis Frontalis Interna:(show top 50) (show all 237)
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