|
Iris hypoplasia and glaucoma
|
C535538 |
|
|
Irons Bhan syndrome
|
C535539 |
|
|
PTB-Associated Splicing Factor
|
D000072670 |
[An RNA splicing factor that also binds DNA. It is essential for pre-mRNA spicing in the formation of early SPLICEOSOMES and catalytic step II. It binds specifically to polypyrimidine tracts in INTRONS and is involved in the regulation of ALTERNATIVE SPLICING by SIGNAL TRANSDUCTION PATHWAYS.
] |
|
MYH9-Related Disorders
|
C535507 |
|
|
Ermine phenotype
|
C535508 |
|
|
Erythema elevatum diutinum
|
C535509 |
|
|
Ankyloglossia
|
D000072676 |
[A severe congenital restriction of TONGUE movement, resulting from fusion or adherence of the tongue to the floor of the mouth. In partial ankyloglossia (tongue-tie) the LINGUAL FRENUM is abnormally short, or is attached too close to the tip of the tongue. OMIM: 106280
] |
|
Epileptic encephalopathy, Lennox-Gastaut type
|
C535500 |
|
|
Epiphyseal dysplasia, multiple, 1
|
C535501 |
|
|
Epiphyseal dysplasia, multiple, 2
|
C535502 |
|
|
Epiphyseal dysplasia, multiple, 3
|
C535503 |
|
|
Epiphyseal dysplasia, multiple, 4
|
C535504 |
|
|
Epiphyseal dysplasia, multiple, 5
|
C535505 |
|
|
Episodic Ataxia, Type 2
|
C535506 |
|
|
mirn206 microRNA, zebrafish
|
C000589537 |
|
|
4',4'',7,7'-tetra-O-methylcupressuflavone
|
C000589538 |
|
|
Renal cysts and diabetes syndrome
|
C535520 |
|
|
Reginato Schiapachasse syndrome
|
C535519 |
|
|
Erythema nodosum, familial
|
C535510 |
|
|
Erythema nodosum, idiopathic
|
C535511 |
|
