Disease Index

9,486 diseases
Madelung deformity, bilateral
human disease
Madelung deformity, unilateral
human disease
Madelung's deformity
Madelung disease, or deformity (MD) is a predominantly bilateral wrist anomaly characterized by shortened and bowed radii and long ulnae leading to dorsal dislocation of the distal ulna and limited mobility of the wrist and elbow
ICD: Q74.0
Madras motor neuron disease
Madras motor neuron disease (MMND) is characterized by weakness and atrophy of limbs, multiple lower cranial nerve palsies and sensorineural hearing loss
Maffucci syndrome
syndrome characterized by the presence of multiple enchondromas (benign growths of cartilage) associated with multiple cavernous hemangiomas and phleboliths
Majeed syndrome
Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis
MeSH: C537839
Majewski's polydactyly syndrome
Human disease
ICD: Q77.2
major hypertriglyceridemia
major induction processes eye anomaly
human disease
Mal de debarquement
medical condition
MeSH: C537840
Mal de Meleda
human disease
malakoplakia
chronic multisystem granulomatous inflammatory disease characterized by the presence of single or multiple soft plaques on various organs of the body
MeSH: D008287
Malan syndrome
human disease
malaria
mosquito-borne infectious disease
MeSH: D008288
male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome
This syndrome is characterized by hypergonadotropic hypogonadism, intellectual deficit, congenital skeletal anomalies involving the cervical spine and superior ribs, and diabetes mellitus
male infertility due to gonadal dysgenesis
human disease
male infertility due to gonadal dysgenesis or sperm disorder
human disease
male infertility due to obstructive azoospermia
human disease
male infertility due to obstructive azoospermia of genetic origin
human disease
male infertility due to sperm disorder
human disease
male infertility due to sperm motility disorder
human disease
male infertility with azoospermia or oligozoospermia due to single gene mutation
male infertility with spermatogenesis disorder
human disease
male infertility with spermatogenesis disorder due to single gene mutation
human disease
malformation of the cerebellar hemispheres
human disease
malformation of the cerebellar vermis
human disease
malformation of the neurenteric canal, spinal cord and column
human disease
malformation syndrome with hamartosis
human disease
malformation syndrome with odontal and/or periodontal component
human disease
malformation syndrome with short stature
human disease
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