Disease Index
9,486 diseasesMichelin tire baby syndrome
human disease
MeSH: C537575
Mickleson syndrome
medical condition
microblepharon-ablephara syndrome
human disease
microbrachycephaly-ptosis-cleft lip syndrome
microcephalic osteodysplastic dysplasia, Saul-Wilson type
congenital abnormality
microcephalic osteodysplastic primordial dwarfism type I
Human disease
microcephalic osteodysplastic primordial dwarfism type II
Human disease
MeSH: C565898
microcephalic primordial dwarfism
human disease
microcephalic primordial dwarfism due to RTTN deficiency
human disease
microcephalic primordial dwarfism due to ZNF335 deficiency
microcephalic primordial dwarfism-insulin resistance syndrome
human disease
microcephalic primordial dwarfism, Alazami type
human disease
microcephalic primordial dwarfism, Toriello type
MeSH: C537321
microcephaly 1, primary, autosomal recessive
human disease
MeSH: C565384
microcephaly lymphoedema chorioretinal dysplasia
syndrome characterized byvariable expression of microcephaly, ocular disorders including chorioretinopathy, congenital lymphedema of the lower limbs, and mild to moderate intellectual disability
MeSH: C537711
microcephaly-albinism-digital anomalies syndrome
Microcephaly - albinism - digital anomalies syndrome is a very rare syndrome associating microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers and agenesia of the distal end of the right big toe
MeSH: C537322
microcephaly-brachydactyly-kyphoscoliosis syndrome
medical condition
MeSH: C536349
microcephaly-brain defect-spasticity-hypernatremia syndrome
human disease
microcephaly-capillary malformation syndrome
human disease
microcephaly-cardiac defect-lung malsegmentation syndrome
Microcephaly - cardiac defect - lung malsegmentation syndrome is a very rare syndrome characterized by the combination of microcephaly, heart defects, renal hypoplasia, lung segmentation defects and cleft palate
microcephaly-cardiomyopathy syndrome
MeSH: C536711
microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome
microcephaly-cervical spine fusion anomalies syndrome
MeSH: C537325
microcephaly-complex motor and sensory axonal neuropathy syndrome
microcephaly-congenital cataract-psoriasiform dermatitis syndrome
human disease
microcephaly-deafness-intellectual disability syndrome
medical condition
MeSH: C537326
microcephaly-digital anomalies-intellectual disability syndrome
, syndactyly of the toes, short fifth fingers with a single flexion crease and absence of the distal interphalangeal crease of the fourth finger) and moderate to severe intellectual deficit
microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type
MeSH: C567850
microcephaly-glomerulonephritis-marfanoid habitus syndrome
This syndrome is characterised by intellectual deficit, marfanoid habitus, microcephaly, and glomerulonephritis
MeSH: C565411
microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome