Also known as:
BARE lymphocyte syndrome, BARE lymphocyte syndrome, type II, BARE lymphocyte syndrome, type II, complementation group B, included, BARE lymphocyte syndrome, type II, complementation group C, included, BARE lymphocyte syndrome, type II, complementation group D, included, BARE lymphocyte syndrome, type II, complementation group E, included, BLS, BLS 2, BLS type II, BLS, type II, BLSII, Bare lymphocyte syndrome, Bare lymphocyte syndrome 2, Bare lymphocyte syndrome type 2, Bare lymphocyte syndrome, type 2, Bare lymphocyte syndrome, type II, Bare lymphocyte syndrome, type II, complementation group A, Bare lymphocyte syndrome, type II, complementation group B, Bare lymphocyte syndrome, type II, complementation group C, Bare lymphocyte syndrome, type II, complementation group D, Bare lymphocyte syndrome, type II, complementation group E, Bls, type 2, HLA class 2-negative SCID, HLA class 2-negative severe combined immunodeficiency, MHC class II expression deficiency, SCID due to absent class II HLA antigens, SCID, HLA CLASS II-NEGATIVE BARE lymphocyte syndrome, type II, complementation group A, included, SCID, HLA Class 2-negative, SCID, HLA Class II-negative, bare lymphocyte syndrome type II, immunodeficiency by defective expression of HLA class 2, immunodeficiency by defective expression of HLA class type 2, major histocompatibility complex class II expression deficiency, severe combined immunodeficiency, HLA Class II-negative, severe combined immunodeficiency, HLA class ii-negative
Also known as:
Dementia, Hereditary Multi-Infarct, Swedish Type, MICROANGIOPATHY AND LEUKOENCEPHALOPATHY, PONTINE, AUTOSOMAL DOMINANT, PADMAL, pontine autosomal dominant microangiopathy with leukoencephalopathy
Also known as:
Richieri Costa-Guion Almeida-Ramos syndrome, Richieri-COSTA/Guion-Almeida syndrome, microbrachycephaly ptosis cleft lip, sao Paulo MCA/Mr syndrome, short stature, intellectual disability, eye anomalies, and cleft Lip/palate, short stature, mental retardation, eye anomalies, and cleft Lip/palate
Also known as:
SWILS, Saul-Wilson syndrome, microcephalic osteodysplastic dysplasia, microcephalic osteodysplastic dysplasia, Saul-Wilson type
Also known as:
MOPD 1, MOPD1, Taybi-Linder syndrome, brachymelic primordial dwarfism, cephaloskeletal dysplasia, low-birth-weight dwarfism with skeletal dysplasia, microcephalic osteodysplastic primordial dwarfism, type 1, microcephalic osteodysplastic primordial dwarfism, type I, osteodysplastic primordial dwarfism type I, osteodysplastic primordial dwarfism, type 1
Also known as:
MOPD II, MOPD type II, MOPD2, Majewski osteodysplastic primordial dwarfism type II, Mopd 2, microcephalic osteodysplastic primordial dwarfism type 2, microcephalic osteodysplastic primordial dwarfism with tooth abnormalities, microcephalic osteodysplastic primordial dwarfism, type 2, microcephalic osteodysplastic primordial dwarfism, type II, osteodysplastic primordial dwarfism type 2, osteodysplastic primordial dwarfism type II, osteodysplastic primordial dwarfism, type 2
Also known as:
MOPD 1, MOPD types I and III, Taybi-Linder syndrome, brachymelic primordial dwarfism, cephaloskeletal dysplasia, low-birth-weight dwarfism with skeletal dysplasia, microcephalic osteodysplastic primordial dwarfism type 1, microcephalic osteodysplastic primordial dwarfism types 1 and 3, microcephalic osteodysplastic primordial dwarfism, Taybi-Linder type, osteodysplastic primordial dwarfism type I, primordial microcephalic dwarfism, Crachami type
Also known as:
Mopd 3, Mopd, Caroline Crachami type, Mopd, Sicilian fairy type, microcephalic osteodysplastic primordial dwarfism, Caroline Crachami type, microcephalic osteodysplastic primordial dwarfism, Sicilian fairy type, microcephalic osteodysplastic primordial dwarfism, type III, osteodysplastic primordial dwarfism, type 3
Also known as:
MCPH10, microcephalic primordial dwarfism, Walsh type, microcephaly 10, primary, autosomal recessive, primary autosomal recessive microcephaly 10
