Disease Index
9,486 diseasesmulticentric osteolysis-nodulosis-arthropathy
rare, autosomal recessive inherited syndrome caused by mutations in the MMP2 gene. It is characterized by the presence of multiple, painless subcutaneous nodules, osteolysis particularly in the hands and feet, osteoporosis, and arthropathy
multicentric osteolysis-nodulosis-arthropathy spectrum
multicentric reticulohistiocytosis
syndrome that is characterized by papulonodular skin lesions containing a proliferation of true macrophages associated with arthritis
multicystic dysplastic kidney
congenital disorder of urinary system
ICD: Q61.4MeSH: D021782
multifocal atrial tachycardia
abnormal heart rhythm, specifically a type of supraventricular tachycardia
Multifocal lymphangioendotheliomatosis
human disease
Multifocal motor neuropathy
Multifocal motor neuropathy (MMN) is a rare acquired immune-mediatedneuropathy characterized clinically by a purely motor deficit with conduction block and asymmetric multifocal weakness, fasciculations, and cramping
ICD: G61.8
multifocal pattern dystrophy simulating fundus flavimaculatus
multifocal stenosing ulceration of the small intestine
human disease
multilocular cystic clear cell renal cell carcinoma
human disease
multiloculated renal cyst
human disease
multiminicore myopathy
Multi-minicore Disease (MmD) is a hereditary neuromuscular disorder characterized by multiple cores on muscle biopsy and clinical features of a congenital myopathy
multinodular goiter
goiter characterized by a multinodular enlargement of the thyroid gland
multinodular goiter-cystic kidney-polydactyly syndrome
Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies
MeSH: C535986
multiple acyl-CoA dehydrogenase deficiency
medical condition
MeSH: D054069
multiple acyl-CoA dehydrogenase deficiency, mild type
human disease
multiple acyl-CoA dehydrogenase deficiency, severe neonatal type
human disease
multiple carboxylase deficiency
human disease
MeSH: D009100
multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
human disease
multiple congenital anomalies-hypotonia-seizures syndrome 1
Human disease
multiple congenital anomalies-hypotonia-seizures syndrome 2
Human disease
multiple congenital anomalies-hypotonia-seizures syndrome 3
Human disease
multiple congenital anomalies/dysmorphic syndrome
human disease
multiple congenital anomalies/dysmorphic syndrome without intellectual disability
human disease
multiple congenital anomalies/dysmorphic syndrome-intellectual disability
human disease
multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome
human disease
multiple cutaneous and mucosal venous malformations
autosomal dominant disease that is characterized by multiple bluish cutaneous or mucosal venous lesions
MeSH: C563977
multiple endocrine neoplasia
human disease
ICD: D44.8MeSH: D009377
multiple endocrine neoplasia type 1
autosomal dominant disease that has material basis in a mutation in the MEN1 tumor suppressor gene and is characterized by over active endocrine glands frequently involving tumors of the parathyroid glands, the pituitary gland, and the pancreas
MeSH: D018761
multiple endocrine neoplasia type 2