Disease Index
9,486 diseasesmultiple endocrine neoplasia type 2A
autosomal dominant disease characterized by medullary carcinoma of the thyroid, pheochromocytoma, hyperparathyroidism, and occasionally cutaneous lichen amyloidosis
MeSH: D018813
multiple endocrine neoplasia type 2B
autosomal dominant disease characterized by medullary thyroid carcinoma, pheochromocytoma, multiple mucosal neuromas and intestinal ganglioneuromas, and often a marfanoid habitus and other skeletal abnormalities
MeSH: D018814
multiple endocrine neoplasia type 4
Human disease
MeSH: C567059
multiple epiphyseal dysplasia
osteochondrodysplasia that has material basis in defective cartilage mineralization into bone which results in irregular ossification centers of the located in hip or located in knee. The disease has symptom fatigue, has symptom joint pain
multiple epiphyseal dysplasia 1
multiple epiphyseal dysplasia that has material basis in heterozygous mutation in the COMP gene on chromosome 19p13
MeSH: C535501
multiple epiphyseal dysplasia 5
multiple epiphyseal dysplasia that has material basis in heterozygous mutation in the MATN3 gene on chromosome 2p24
MeSH: C535505
multiple epiphyseal dysplasia 7
multiple epiphyseal dysplasia that has material basis in homozygous mutation in the CANT1 gene on chromosome 17q25
multiple epiphyseal dysplasia and pseudoachondroplasia
human disease
multiple epiphyseal dysplasia due to collagen 9 anomaly
multiple epiphyseal dysplasia that has material basis in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3)
multiple epiphyseal dysplasia, Beighton type
Multiple epiphyseal dysplasia, Beighton type is a skeletal dysplasia characterized by epiphyseal dysplasia (usually mild) associated with progressive myopia, retinal thinning, crenated cataracts, conductive deafness, and stubby digits
multiple epiphyseal dysplasia, Lowry type
human disease
MeSH: C563291
multiple epiphyseal dysplasia, with miniepiphyses
human disease
MeSH: C563735
multiple epiphyseal dysplasia, with severe proximal femoral dysplasia
MeSH: C563736
multiple familial trichoepithelioma
human disease
MeSH: C536552
multiple fibroadenoma of the breast
Mammary polyadenomatosis is characterised by the presence in both breasts of multiple voluminous fibroadenomas with heterogeneous echo patterns
multiple hamartoma syndrome
syndrome characterized as a spectrum of disorders (Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, PTEN-related Proteus syndrome, and Proteus-like syndrome) caused by germline mutations of the PTEN gene
MeSH: D006223
multiple intestinal atresia
Human disease
MeSH: C562441
multiple metaphyseal dysplasia
human disease
multiple mitochondrial DNA deletion syndrome
human disease
multiple mitochondrial dysfunctions syndrome 1
Human disease
multiple mitochondrial dysfunctions syndrome 2
Human disease
multiple mitochondrial dysfunctions syndrome 3
Human disease
multiple mitochondrial dysfunctions syndrome 4
human disease
multiple mitochondrial dysfunctions syndrome 5
human disease
multiple mitochondrial dysfunctions syndrome 6
human disease
multiple myeloma
cancer of plasma cells
MeSH: D009101
multiple paragangliomas associated with polycythemia
human disease
multiple polyglandular tumor
human disease
multiple pterygium syndrome
Human disease
MeSH: C537377
multiple pterygium-malignant hyperthermia syndrome
MeSH: C565679