Mccune-Albright Syndrome (MAS)

Alias:
Polyostotic Fibrous Dysplasia
Mass Syndrome
Fibrous Dysplasia of Bone
Overlap Connective Tissue Disease
Osteitis Fibrosa Disseminata
Mass Phenotype
Mas
Gonadotropin-Independent Female-Limited Sexual Precocity
Mccune Albright Syndrome
Albright's Syndrome
Albright Syndrome
Octd
Fibrous Dysplasia with Pigmentary Skin Changes and Precocious Puberty
Albright's Syndrome with Precocious Puberty
Mccune-Albright Syndrome, Somatic, Mosaic
Albright-Mccune-Sternberg Syndrome
Fibrous Dysplasia, Polyostotic
Fibrous Dysplasia Polyostotic
Albright-Sternberg Syndrome
Albright's Disease of Bone
Albright's Disease
Pofd
Pfd
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Mccune-Albright Syndrome, also known as polyostotic fibrous dysplasia, is related to fibrous dysplasia and precocious puberty, male-limited. An important gene associated with Mccune-Albright Syndrome is GNAS (GNAS Complex Locus), and among its related pathways/superpathways are ERK Signaling and Nanog in Mammalian ESC Pluripotency. The drugs Denosumab and Risedronic acid have been mentioned in the context of this disorder. Affiliated tissues include bone and skin, and related phenotypes are fibrous dysplasia of the bones and precocious puberty
Related ID:
MESH:D005359
ICD11:1704766818

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Child
1-9/1000000
32
336
77

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
Journal
Year
IF
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