Experimental Factor Ontology
3201 terms(s) returned
| Term Type: | Record: 2051 to 2100 of 3201 Records | Page: 42 of 65, First Previous Next Last | Show Records Per Page |
- microbrachycephaly-ptosis-cleft lip syndrome
- microcephalic osteodysplastic dysplasia, Saul-Wilson type
- microcephalic osteodysplastic primordial dwarfism
- microcephalic osteodysplastic primordial dwarfism type I
- microcephalic osteodysplastic primordial dwarfism type II
- microcephalic osteodysplastic primordial dwarfism types I and III
- microcephalic primordial dwarfism
- microcephalic primordial dwarfism due to RTTN deficiency
- microcephalic primordial dwarfism due to ZNF335 deficiency
- microcephalic primordial dwarfism, Alazami type
- microcephalic primordial dwarfism, Toriello type
- microcephalic primordial dwarfism-insulin resistance syndrome
- microcephaly
- microcephaly 1, primary, autosomal recessive
- microcephaly 27, primary, autosomal dominant
- microcephaly 28, primary, autosomal recessive
- microcephaly 30, primary, autosomal recessive
- microcephaly and chorioretinopathy
- microcephaly and chorioretinopathy 1
- microcephaly and chorioretinopathy 3
- microcephaly with intellectual disability
- microcephaly with lissencephaly and/or hydranencephaly
- microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
- microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum
- microcephaly, developmental delay, and brittle hair syndrome
- microcephaly, epilepsy, and diabetes syndrome
- microcephaly, epilepsy, and diabetes syndrome 1
- microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome
- microcephaly, growth deficiency, seizures, and brain malformations
- microcephaly, growth restriction and increased sister chromatid exchange
- microcephaly, growth restriction, and increased sister chromatid exchange 2
- microcephaly, seizures, and developmental delay
- microcephaly, short stature, and limb abnormalities
- microcephaly-albinism-digital anomalies syndrome
- microcephaly-brachydactyly-kyphoscoliosis syndrome
- microcephaly-brain defect-spasticity-hypernatremia syndrome
- microcephaly-capillary malformation syndrome
- microcephaly-cardiac defect-lung malsegmentation syndrome
- microcephaly-cardiomyopathy syndrome
- microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome
- microcephaly-cervical spine fusion anomalies syndrome
- microcephaly-cleft palate syndrome
- microcephaly-complex motor and sensory axonal neuropathy syndrome
- microcephaly-congenital cataract-psoriasiform dermatitis syndrome
- microcephaly-deafness-intellectual disability syndrome
- microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type
- microcephaly-glomerulonephritis-marfanoid habitus syndrome
- microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome
- microcephaly-microcornea syndrome, Seemanova type
- microcephaly-micromelia syndrome
