Disease Index
9,486 diseasesacquired kinky hair syndrome
acquired lipodystrophy
instance of lipodystrophy (disease) that is acquired during the lifetime of the individual
acquired monoclonal Ig light chain-associated Fanconi syndrome
acquired motor neuron disease
instance of motor neuron disease that is acquired during the lifetime of the individual
acquired neuromuscular junction disease
instance of neuromuscular junction disease that is acquired during the lifetime of the individual
acquired neutropenia
instance of neutropenia that is acquired during the lifetime of the individual
acquired peripheral movement disorder
human disease
acquired peripheral neuropathy
instance of peripheral neuropathy that is acquired during the lifetime of the individual
acquired pituitary hormone deficiency
instance of hypopituitarism that is acquired during the lifetime of the individual
acquired polycythemia
Human disease
acquired porencephaly
instance of porencephaly that is acquired during the lifetime of the individual
acquired premature ovarian failure
human disease
acquired prothrombin deficiency
instance of prothrombin deficiency that is acquired during the lifetime of the individual
MeSH: C538174
acquired pseudoxanthoma elasticum
instance of pseudoxanthoma elasticum that is acquired during the lifetime of the individual
acquired schizencephaly
instance of schizencephaly that is acquired during the lifetime of the individual
acquired secondary polycythemia
instance of secondary polycythemia that is acquired during the lifetime of the individual
acquired sensory ganglionopathy
human disease
acquired skeletal muscle disease
instance of skeletal muscle disease that is acquired during the lifetime of the individual
acquired thrombotic thrombocytopenic purpura
MeSH: C536901
acquired von Willebrand syndrome
human disease
acral dystrophic epidermolysis bullosa
Acral dystrophic epidermolysis bullosa is a very rare subtype of dystrophic epidermolysis bullosa (DEB, see this term) characterized by blistering confined primarily to the hands and feet
acral peeling skin syndrome
autosomal recessive genodermatosis characterized by the shedding of the outer epidermis
MeSH: C536316
Acral persistent papular mucinosis
medical condition
acral self-healing collodion baby
Acral self-healing collodion baby (SHCB) is a variant of SHCB (see this term) characterized by the presence at birth of a collodion membrane only at the extremities
acrania
medical condition
ICD: Q00.0
Acro-renal-mandibular syndrome
medical condition
MeSH: C535665
acro-renal-ocular syndrome
related disorders including Okihiro syndrome and Holt-Oram syndrome (see these terms). Transmission is autosomal dominant.
acrocallosal syndrome
syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation
ICD: Q04.0MeSH: D055673
acrocapitofemoral dysplasia
Human disease
MeSH: C564334
acrocardiofacial syndrome
Acro-cardio-facial syndrome (ACFS) is a rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, cleft lip/palate, congenital heart defect (CHD), genital anomalies, and intellectual deficit
MeSH: C563936