Disease Index
9,486 diseasesectrodactyly and ectodermal dysplasia without cleft lip/palate
human disease
MeSH: C565065
ectrodactyly-cleft palate syndrome
human disease
MeSH: C565064
ectrodactyly-polydactyly syndrome
human disease
MeSH: C565601
ectrodactyly–ectodermal dysplasia–cleft syndrome
autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate)
MeSH: C536189
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
EEC syndrome characterized by autosomal dominant inheritance that has material basis in variation in the chromosome region 7q11.2-q21.3
MeSH: C536189
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3
Human disease
MeSH: C536189
EDICT syndrome
Edinburgh malformation syndrome
human disease
MeSH: C563051
Edwards syndrome
human disease
MeSH: D000073842
EEC syndrome and related syndrome
human disease
EEM syndrome
medical condition
ICD: Q82.4MeSH: C536190
Efavirenz, poor metabolism of
human disease
Ehlers-Danlos syndrome
group of genetic connective tissue disorders
MeSH: D004535
Ehlers-Danlos syndrome classic-like 2
human disease
Ehlers-Danlos syndrome due to tenascin-X deficiency
human disease
MeSH: C536193
Ehlers-Danlos syndrome progeroid type
Human disease
MeSH: C536201
Ehlers-Danlos syndrome type 2
human disease
MeSH: C536195
Ehlers-Danlos syndrome type 7A
human disease
Ehlers-Danlos syndrome type 7B
human disease
MeSH: C565061
Ehlers-Danlos syndrome with periventricular heterotopia
Ehlers-Danlos syndrome, arthrochalasis type
MeSH: C562625
Ehlers-Danlos syndrome, cardiac valvular type
MeSH: C536200
Ehlers-Danlos syndrome, dermatosparaxis type
human disease
MeSH: C567527
Ehlers-Danlos syndrome, fibronectinemic type
MeSH: C565600
Ehlers-Danlos syndrome, kyphoscoliotic and deafness type
Ehlers-Danlos syndrome, musculocontractural type
MeSH: C000600608
Ehlers-Danlos syndrome, periodontitis type
Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility
MeSH: C562626
Ehlers-Danlos syndrome, spondylocheirodysplastic type
human disease
MeSH: C567340
Ehlers-Danlos syndrome, vascular-like type
Ehlers-Danlos, vascular-like type is an adult-onset form of Ehlers-Danlos syndrome characterized by spontaneous dissection of medium-sized arteries during young adulthood, including mainly the iliac, femoral, and renal arteries
Ehlers-Danlos/osteogenesis imperfecta syndrome
MeSH: C565178