Son Results

SON

SON DNA binding protein
04/24/2019

ATG9B

autophagy related 9B

DONSON

downstream neighbor of SON

Wilson disease

MONDO_0010200 Condition
Cerebral pseudosclerosis
03/27/2019

Mowat-Wilson syndrome

MONDO_0009341 Condition
microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease
10/10/2018

Borjeson-Forssman-Lehmann syndrome

MONDO_0010537 Condition
intellectual deficiency-epilepsy-endocrine disorders syndrome
10/10/2018

Christianson syndrome

MONDO_0010278 Condition
X-linked Angelman-like syndrome
05/02/2018

autosomal recessive early-onset Parkinson disease 6

MONDO_0011613 Condition
autosomal recessive early-onset Parkinson disease type 6
11/13/2018

Simpson-Golabi-Behmel syndrome

MONDO_0010731 Condition
X-linked dysplasia gigantism syndrome
01/04/2019

Wolcott-Rallison syndrome

MONDO_0009192 Condition
Early-onset diabetes mellitus with multiple epiphyseal dysplasia
05/31/2017

Johanson-Blizzard syndrome

MONDO_0009479 Condition
JBS
10/23/2018

Rothmund-Thomson syndrome

MONDO_0010002 Condition
Poikiloderma of Rothmund-Thomson
10/11/2018

juvenile onset Parkinson disease 19A

MONDO_0014231 Condition
juvenile onset Parkinson disease type 19A
10/17/2018

cortisone reductase deficiency 1

MONDO_0011503 Condition
cortisone reductase deficiency type 1
10/23/2018

parkinsonian-pyramidal syndrome

MONDO_0009830 Condition
pallidopyramidal syndrome
05/31/2017

early-onset parkinsonism-intellectual disability syndrome

MONDO_0010709 Condition
Laxova-Opitz syndrome
06/04/2018

Sjogren-Larsson syndrome

MONDO_0010031 Condition
Sjogren-Larsson syndrome (disorder)
10/18/2018

autosomal recessive early-onset Parkinson disease 7

MONDO_0011658 Condition
autosomal recessive early-onset Parkinson disease type 7
10/18/2018

Wolff-Parkinson-white syndrome (disease)

MONDO_0008685 Condition
Anomalous A-V excitation

obsolete rare genetic parkinsonian disorder

MONDO_0017660 Condition
Rare genetic hypokinetic movement disorder

Pierson syndrome

MONDO_0012184 Condition
microcoria-congenital nephrosis syndrome

obsolete Stevens-Johnson syndrome

MONDO_0012065 Condition