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SHCB
MCID: SLF015
MIFTS: 32

Self-Improving Collodion Baby (SHCB)

Categories: Eye diseases, Fetal diseases, Rare diseases, Skin diseases
Genes Tissues Related diseases Publications Pathways Symptoms & Phenotypes Drugs
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Aliases & Classifications for Self-Improving Collodion Baby

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MalaCards integrated aliases for Self-Improving Collodion Baby:

Name: Self-Improving Collodion Baby 58
Self-Healing Collodion Baby 58 71
Self-Improving Congenital Ichthyosis 58
Shcb 58
Sici 58

Characteristics:

Orphanet epidemiological data:

58
self-improving collodion baby
Inheritance: Autosomal recessive; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal;

Classifications:

MalaCards categories:
Global: Fetal diseases Rare diseases
Anatomical: Eye diseases Skin diseases
See all MalaCards categories (disease lists)
ICD10: 33
Orphanet: 58  
Rare eye diseases
Rare skin diseases
Developmental anomalies during embryogenesis


External Ids:

ICD10 via Orphanet 33 Q80.2
UMLS via Orphanet 72 C1855789
Orphanet 58 ORPHA281122
UMLS 71 C1855789
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Summaries for Self-Improving Collodion Baby

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MalaCards based summary : Self-Improving Collodion Baby, also known as self-healing collodion baby, is related to ichthyosis, congenital, autosomal recessive 2 and ichthyosis, congenital, autosomal recessive 1. An important gene associated with Self-Improving Collodion Baby is ALOX12B (Arachidonate 12-Lipoxygenase, 12R Type), and among its related pathways/superpathways is Prostaglandin 2 biosynthesis and metabolism FM. The drugs Adrenergic Agents and Atomoxetine Hydrochloride have been mentioned in the context of this disorder. Affiliated tissues include brain, cortex and eye, and related phenotypes are ichthyosis and limitation of joint mobility

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Related Diseases for Self-Improving Collodion Baby

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Diseases related to Self-Improving Collodion Baby via text searches within MalaCards or GeneCards Suite gene sharing:

(show all 41)
# Related Disease Score Top Affiliating Genes
1 ichthyosis, congenital, autosomal recessive 2 32.0 ALOXE3 ALOX12B
2 ichthyosis, congenital, autosomal recessive 1 31.0 TGM1 ALOXE3 ALOX12B
3 ichthyosis 29.7 TGM1 ALOXE3 ALOX12B
4 autosomal recessive congenital ichthyosis 29.5 TGM1 ALOXE3 ALOX12B
5 ichthyosis, congenital, autosomal recessive 3 12.2
6 acral self-healing collodion baby 11.2
7 ischemia 10.4
8 hypertelorism 10.2
9 dowling-degos disease 1 10.2
10 chromosome 2q35 duplication syndrome 10.2
11 brachydactyly 10.2
12 keratosis 10.2
13 skin atrophy 10.2
14 alopecia 10.2
15 peripheral vascular disease 10.2
16 autosomal recessive cerebellar ataxia 10.2
17 coronary stenosis 10.2
18 arteries, anomalies of 10.1
19 atrial standstill 1 10.1
20 hypercholesterolemia, familial, 1 10.1
21 stroke, ischemic 10.1
22 aortic valve disease 2 10.1
23 hyperlipoproteinemia, type iii 10.1
24 lipoprotein quantitative trait locus 10.1
25 patent foramen ovale 10.1
26 vascular disease 10.1
27 chronic kidney disease 10.1
28 intermediate coronary syndrome 10.1
29 pulmonary embolism 10.1
30 cardiogenic shock 10.1
31 acrokeratosis verruciformis 9.6 TGM1 ALOX12B
32 bleeding disorder, platelet-type, 8 9.4 ALOXE3 ALOX12B
33 epidermolytic hyperkeratosis 9.4 TGM1 ALOXE3
34 skin disease 9.4 TGM1 ALOX12B
35 ichthyosis, congenital, autosomal recessive 7 9.2 TGM1 ALOXE3 ALOX12B
36 x-linked chondrodysplasia punctata 2 9.2 TGM1 ALOXE3 ALOX12B
37 ectropion 9.2 TGM1 ALOXE3 ALOX12B
38 ichthyosis, x-linked 9.2 TGM1 ALOXE3 ALOX12B
39 ichthyosis, congenital, autosomal recessive 4b 9.2 TGM1 ALOXE3 ALOX12B
40 eyelid disease 9.1 TGM1 ALOXE3 ALOX12B
41 ichthyosis vulgaris 9.1 TGM1 ALOXE3 ALOX12B

Graphical network of the top 20 diseases related to Self-Improving Collodion Baby:



Diseases related to Self-Improving Collodion Baby
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Symptoms & Phenotypes for Self-Improving Collodion Baby

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Human phenotypes related to Self-Improving Collodion Baby:

58 31
# Description HPO Frequency Orphanet Frequency HPO Source Accession
1 ichthyosis 58 31 hallmark (90%) Very frequent (99-80%) HP:0008064
2 limitation of joint mobility 58 31 hallmark (90%) Very frequent (99-80%) HP:0001376

MGI Mouse Phenotypes related to Self-Improving Collodion Baby:

45
# Description MGI Source Accession Score Top Affiliating Genes
1 integument MP:0010771 8.8 ALOX12B ALOXE3 TGM1
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Drugs & Therapeutics for Self-Improving Collodion Baby

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Drugs for Self-Improving Collodion Baby (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(show all 19)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1 Adrenergic Agents Phase 3
2 Atomoxetine Hydrochloride Phase 3
3 Pharmaceutical Solutions Phase 2
4 Orange Approved Phase 1
5 GABA Modulators Phase 1
6
Methamphetamine Approved, Illicit 537-46-2 10836
7
Methylphenidate Approved, Investigational 113-45-1 4158
8
Dopamine Approved 51-61-6, 62-31-7 681
9
Ethanol Approved 64-17-5 702
10
Acetylcholine Approved, Investigational 51-84-3 187
11
Glutamic acid Approved, Nutraceutical 56-86-0 33032
12 Nabiximols Investigational 56575-23-6
13 Dopamine Agents
14 Analgesics
15 Anesthetics
16 Central Nervous System Stimulants
17 Neurotransmitter Agents
18 Cholinergic Agents
19 Botulinum Toxins

Interventional clinical trials:

(show all 29)
# Name Status NCT ID Phase Drugs
1 Antispastic Effect of Transcranial Magnetic Stimulation in Patients With Cerebral and Spinal Spasticity Unknown status NCT01786005 Phase 4
2 Cortical Excitability: Phenotype and Biomarker in ADHD Therapy Unknown status NCT01330693 Phase 3 Atomoxetine;Sugar Pill
3 Effect of Transcranial Direct Current Stimulation (tDCS) Optimized Protocol for the Treatment of Migraine Unknown status NCT02562196 Phase 2
4 Optimizing the Effect of Transcranial Direct Current Stimulation (tDCS) for the Treatment of Migraine Unknown status NCT02562222 Phase 2
5 A Phase I Single Site, Single Dose, Randomised, Double-blind, Placebo Controlled 3-way Cross-over Biomarker Study Investigating the Effect of the GABA Modulator AZD7325 on Short Interval Intracortical Inhibition (SICI) in Healthy Volunteers Completed NCT02135198 Phase 1 2 mg AZD7325;10 mg AZD7325;Placebo
6 Effect of rTMS Over the Medial Cerebellum on Negative Symptoms and Cognitive Dysmetria in Subjects With Treatment Refractory Schizophrenia Unknown status NCT02242578
7 Effects of Non-invasive Stimulation on Central Nervous System Excitability of Healthy Volunteers Unknown status NCT02659826
8 Evaluating the Effect of Methylphenidate on Intracortical Inhibition in Methamphetamine Abusers Comorbid With Attention Deficit Disorder With Hyperactivity(ADHD) in TMS Unit, Neurcognitive Lab, Iranian National Center for Addiction Studies (INCAS), in 2012. A Randomized, Controlled Trial Unknown status NCT01651169
9 Efficacy of the Non-invasive Brain Stimulation Techniques for Lower Limb Recovery in Stroke Patients Unknown status NCT02920333
10 The Effects of Repetitive Transcranial Magnetic Stimulation in Healthy Human Subjects Completed NCT00658307
11 Prospective Study Evaluating the Routine Standard Use of Fractional Flow Reserve and Disagreement With Guideline Recommendations: a Nationwide Study Completed NCT03082989
12 Impaired Motor Learning and LTP/LTD-like Plasticity in Dystonia, Are Associated With Abnormal Modulation of Cortical Excitability by Somatosensory Volleys Completed NCT00102999
13 Role of the Cortical Medial Frontal Areas in Blepharospasm Completed NCT00500799
14 Effects of Non-invasive Cerebellar Stimulation on Motor Learning and Cortical Electrical Activity of Healthy Individuals Completed NCT02559518
15 Effects of the Visual Stimulation on the Motor and Visual Cortex in Migraneurs With and Without Aura Completed NCT02564822
16 Investigating the Plastic Effects of Repetitive Paired Associative Stimulation (rPAS) in Dystonia Completed NCT01888926
17 Rehabilitative Trial With Transcranial Direct Current Stimulation (tDCS) in Amyotrophic Lateral Sclerosis Completed NCT03293394
18 The Role of SAtivex® Associated With Robotic-Rehabilitation in Improving the Motor Performances of Multiple Sclerosis Patients (SARR) Completed NCT03186664 Sativex
19 Enhancing Interhemispheric Disinhibition Between Motor Cortices Using Bilateral Brain Stimulation Completed NCT00396890
20 The Effect of Surround Inhibition During Phasic Compared to Tonic Voluntary Finger Movement in Focal Hand Dystonia Completed NCT00376753
21 Ethanol Response in Essential Tremor: Clinical and Neurophysiological Correlates Completed NCT01200966
22 Detailed Evaluation of the Neurophysiology of Surround Inhibition in the Human Motor Cortex Recruiting NCT03018262 Early Phase 1
23 Targeting Brain Physiology to Treat Neuropsychiatric Symptoms of Dementia Using TMS-EEG and tDCS Recruiting NCT03846492
24 Movement-Based Training for Children With ADHD: A Feasibility Study Recruiting NCT02234557
25 Effects of Ongoing Movement-Based Mindfulness Training for Children With ADHD Enrolling by invitation NCT03434509
26 Metabotropic Receptors For Glutamate Type 3 In Parkinson's Disease: Clinical And Neurophysiological Correlations Not yet recruiting NCT03998787
27 Clinical Relevance of miR-142-3p as Potential Biomarker of Synaptopathy in Multiple Sclerosis Not yet recruiting NCT03999788
28 Physiological Effects of Botulinum Toxin Therapy in Primary Cervical Dystonia Terminated NCT02837185
29 Interhemispheric Interaction of Parieto-Motor Cortico-Cortical Plasticity in Human Brain Withdrawn NCT03253731

Search NIH Clinical Center for Self-Improving Collodion Baby

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Genetic Tests for Self-Improving Collodion Baby

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Anatomical Context for Self-Improving Collodion Baby

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MalaCards organs/tissues related to Self-Improving Collodion Baby:

40
Brain, Cortex, Eye, Cerebellum, Skin
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Publications for Self-Improving Collodion Baby

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Articles related to Self-Improving Collodion Baby:

(show all 23)
# Title Authors PMID Year
1
Genotypic and clinical spectrum of self-improving collodion ichthyosis: ALOX12B, ALOXE3, and TGM1 mutations in Scandinavian patients. 61 6
19890349 2010
2
Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B. 6
19131948 2009
3
Self-healing collodion membrane and mild nonbullous congenital ichthyosiform erythroderma due to 2 novel mutations in the ALOX12B gene. 6
18347291 2008
4
Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. 6
17139268 2007
5
Mutation spectrum and functional analysis of epidermis-type lipoxygenases in patients with autosomal recessive congenital ichthyosis. 6
16116617 2005
6
Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1. 6
11773004 2002
7
Autosomal Recessive Congenital Ichthyosis 6
20301593 2001
8
A case of self-improving collodion ichthyosis in Vietnam. 61
32105361 2020
9
Acral self-healing collodion baby. 61
28735267 2017
10
Acral self-healing collodion baby: A case series. 61
28492026 2016
11
Self-healing Collodion Baby: A New Mutation in the ALOX12B Gene. 61
26922124 2016
12
Inherited ichthyosis: Non-syndromic forms. 61
26945532 2016
13
Two Cases of Autosomal Recessive Congenital Ichthyosis due to CYP4F22 Mutations: Expanding the Genotype of Self-Healing Collodion Baby. 61
26646773 2016
14
Otologic Manifestations of Autosomal Recessive Congenital Ichthyosis in Children. 61
26206273 2015
15
Scanning electron microscopy of the collodion membrane from a self-healing collodion baby. 61
26375232 2015
16
Novel TGM1 missense mutation p.Arg727Gln in a case of self-healing collodion baby. 61
24419105 2014
17
Autosomal recessive congenital ichthyosis. 61
23562412 2013
18
Self-healing collodion baby. 61
20334876 2010
19
Genotype-phenotype correlations with TGM1: clustering of mutations in the bathing suit ichthyosis and self-healing collodion baby variants of lamellar ichthyosis. 61
19863506 2010
20
Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutation. 61
19500103 2009
21
Self-healing collodion baby: a dynamic phenotype explained by a particular transglutaminase-1 mutation. 61
12542526 2003
22
Koraxitrachitic syndrome: a syndromic form of self-healing collodion baby with residual dappled atrophy of the derma. 61
10508988 1999
23
Self-healing collodion baby: evidence for autosomal recessive inheritance. 61
1603745 1992
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Variations for Self-Improving Collodion Baby

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Expression for Self-Improving Collodion Baby

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Search GEO for disease gene expression data for Self-Improving Collodion Baby.
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Pathways for Self-Improving Collodion Baby

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Pathways related to Self-Improving Collodion Baby according to GeneCards Suite gene sharing:

# Super pathways Score Top Affiliating Genes
1
Prostaglandin 2 biosynthesis and metabolism FM 22
9.98 ALOXE3 ALOX12B
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GO Terms for Self-Improving Collodion Baby

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Biological processes related to Self-Improving Collodion Baby according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 fatty acid metabolic process GO:0006631 9.43 ALOXE3 ALOX12B
2 sphingolipid metabolic process GO:0006665 9.4 ALOXE3 ALOX12B
3 arachidonic acid metabolic process GO:0019369 9.37 ALOXE3 ALOX12B
4 ceramide biosynthetic process GO:0046513 9.32 ALOXE3 ALOX12B
5 establishment of skin barrier GO:0061436 9.26 ALOXE3 ALOX12B
6 linoleic acid metabolic process GO:0043651 9.16 ALOXE3 ALOX12B
7 lipoxygenase pathway GO:0019372 8.96 ALOXE3 ALOX12B
8 hepoxilin biosynthetic process GO:0051122 8.62 ALOXE3 ALOX12B

Molecular functions related to Self-Improving Collodion Baby according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 lyase activity GO:0016829 9.32 ALOXE3 ALOX12B
2 iron ion binding GO:0005506 9.26 ALOXE3 ALOX12B
3 isomerase activity GO:0016853 9.16 ALOXE3 ALOX12B
4 dioxygenase activity GO:0051213 8.96 ALOXE3 ALOX12B
5 oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen GO:0016702 8.62 ALOXE3 ALOX12B
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Sources for Self-Improving Collodion Baby

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3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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