Polymicrogyria and Schizencephaly (Version 0.195)

List	Entity	Reviews	Mode of inheritance	Details
Filter Entities 86 Entitiess
Green List (high evidence)	ADGRG1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Polymicrogyria, bilateral frontoparietal, MIM#606854 Tags 5'UTR
Green List (high evidence)	AKT3	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2 (MIM#615937) Tags
Green List (high evidence)	ARX	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	ATP1A2	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies, MIM# 619602 Developmental and epileptic encephalopathy 98 , MIM#619605 Tags
Green List (high evidence)	ATP1A3	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Polymicrogyria epilepsy developmental delay Tags
Green List (high evidence)	BICD2	2 reviews 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Spinal muscular atrophy, lower extremity-predominant, 2B. MIM: 618291 Tags
Green List (high evidence)	CCND2	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert list Expert Review Green Phenotypes Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3 MIM#615938 Tags
Green List (high evidence)	COL18A1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Knobloch syndrome, type 1 MIM# 267750 Tags
Green List (high evidence)	COL3A1	1 review 1 green	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Polymicrogyria with or without vascular-type ehlers-danlos syndrome, MIM # 618343 Ehlers-Danlos syndrome, vascular type, MIM# 130050 Tags
Green List (high evidence)	COL4A1	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes 1. Angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps, 611773 AD 2. Brain small vessel disease with or without ocular anomalies, 175780, AD 3. Microangiopathy and leukoencephalopathy, pontine, autosomal dominant, 618564, AD 4. ?Retinal arteries, tortuosity of, 180000, AD 5. {Hemorrhage, intracerebral, susceptibility to}, 614519 Tags
Green List (high evidence)	CSMD1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes complex neurodevelopmental disorder MONDO:0100038 Tags
Green List (high evidence)	DEPDC5	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder, DEPDC5-related, MONDO:0700092 Tags
Green List (high evidence)	DYNC1H1	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	EML1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Band heterotopia (MIM# 600348) Tags
Green List (high evidence)	GPSM2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert list Expert Review Green Phenotypes Chudley-McCullough syndrome MIM#604213 Tags
Green List (high evidence)	GRIN1	2 reviews 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant, MIM# 614254 Tags
Green List (high evidence)	GRIN2B	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes GRIN2B-related neurodevelopmental disorder Mental retardation, autosomal dominant 6, MIM# 613970 Tags
Green List (high evidence)	HSD17B4	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes D-bifunctional protein deficiency - MIM#261515 Tags
Green List (high evidence)	KIF1BP	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Goldberg-Shprintzen megacolon syndrome MIM#609460 Tags new gene name
Green List (high evidence)	KIF26A	2 reviews 2 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cortical dysplasia, complex, with other brain malformations 11, MIM# 620156 Tags
Green List (high evidence)	KIF5C	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Cortical dysplasia, complex, with other brain malformations 2, MIM# 615282 Tags
Green List (high evidence)	LAMC3	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Cortical malformations, occipital, MIM#614115 Tags
Green List (high evidence)	MAN2C1	2 reviews 2 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Research Phenotypes Congenital disorder of deglycosylation 2, MIM# 619775 Tags
Green List (high evidence)	MAP1B	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Intellectual disability seizures PVNH dysmorphic features Periventricular nodular heterotopia 9, MIM# 618918 Tags
Green List (high evidence)	MAPK8IP3	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with or without variable brain abnormalities OMIM# 605431 Tags
Green List (high evidence)	MAST1	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations, MIM# 618273 Tags
Green List (high evidence)	NDE1	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	NEDD4L	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Periventricular nodular heterotopia 7, MIM# 617201 polymicrogyria syndactyly Tags
Green List (high evidence)	OCLN	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PEX1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Peroxisome biogenesis disorder 1A (Zellweger) (MIM#214100) Tags
Green List (high evidence)	PEX6	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Peroxisome biogenesis disorder 4A (Zellweger) (MIM#614862) Tags
Green List (high evidence)	PIK3CA	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PIK3R2	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	PTEN	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Macrocephaly/autism syndrome, MIM# 605309 Tags
Green List (high evidence)	RAB18	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Warburg micro syndrome 3, MIM# 614222 Tags
Green List (high evidence)	RAB3GAP1	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Warburg micro syndrome 1, MIM# 600118 Tags
Green List (high evidence)	RAB3GAP2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Warburg micro syndrome 2 614225 Tags
Green List (high evidence)	RAC1	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Mental retardation, autosomal dominant 48, MIM# 617751 Tags
Green List (high evidence)	RAC3	1 review 1 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with structural brain anomalies and dysmorphic facies, MIM#618577 Tags
Green List (high evidence)	RTTN	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	SCN3A	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Polymicrogyria epileptic encephalopathy Tags
Green List (high evidence)	SHMT2	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities (NEDCASB), MIM#619121 Congenital microcephaly Infantile axial hypotonia Spastic paraparesis Global developmental delay Intellectual disability Abnormality of the corpus callosum Abnormal cortical gyration Hypertrophic cardiomyopathy Abnormality of the face Proximal placement of thumb 2-3 toe syndactyly Tags
Green List (high evidence)	SNAP29	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome (MIM#609528) Tags
Green List (high evidence)	TCP1	2 reviews 2 green	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Intellectual developmental disorder with polymicrogyria and seizures, MIM# 621021 Tags
Green List (high evidence)	TMX2	2 reviews 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity MIM#618730 Tags
Green List (high evidence)	TUBA1A	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	TUBB	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	TUBB2B	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	TUBB3	0 reviews	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Tags
Green List (high evidence)	WDR62	1 review 1 green	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Green Victorian Clinical Genetics Services Phenotypes Microcephaly 2, primary, autosomal recessive, with or without cortical malformations, MIM# 604317 MONDO:0011435 Tags
Amber List (moderate evidence)	AHI1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes Joubert syndrome 3, MIM# 608629 Tags
Amber List (moderate evidence)	ASTN1	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes Polymicrogyria hypoplastic corpus callosum Tags
Amber List (moderate evidence)	COL4A2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Literature Phenotypes Brain small vessel disease 2, MIM#614483 Tags
Amber List (moderate evidence)	EMX2	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes Schizencephaly MIM# 269160 Tags disputed
Amber List (moderate evidence)	FIG4	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes Polymicrogyria with epilepsy MIM# 612691 Tags
Amber List (moderate evidence)	L1CAM	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes L1CAM-related disease Tags
Amber List (moderate evidence)	MED25	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Basel-Vanagait-Smirin-Yosef syndrome, MIM# 616449 Tags
Amber List (moderate evidence)	MFN2	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Mitochondrial disease, MONDO:0044970, MFN2-related Tags
Amber List (moderate evidence)	NHEJ1	1 review	Unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation (MIM# 611291) Tags
Amber List (moderate evidence)	NSDHL	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes CK syndrome 300831 Tags
Amber List (moderate evidence)	PAX6	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes ?Coloboma of optic nerve MIM# 120430 ?Coloboma, ocular MIM# 120200 ?Morning glory disc anomaly MIM# 120430 Aniridia MIM# 106210 Anterior segment dysgenesis 5, multiple subtypes MIM# 604229 Cataract with late-onset corneal dystrophy MIM# 106210 Foveal hypoplasia 1 MIM# 136520 Keratitis MIM# 148190 Optic nerve hypoplasia MIM# 165550 Tags
Amber List (moderate evidence)	PEX10	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 6A (Zellweger) (MIM#614870) Tags
Amber List (moderate evidence)	PEX12	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 3A (Zellweger) (MIM#614859) Tags
Amber List (moderate evidence)	PEX13	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 11A (Zellweger) (MIM#614883) Tags
Amber List (moderate evidence)	PEX14	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876 Tags
Amber List (moderate evidence)	PEX16	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876 Tags
Amber List (moderate evidence)	PEX19	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 12A (Zellweger) MIM#614886 Tags
Amber List (moderate evidence)	PEX2	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 5A (Zellweger) MIM#614866 Tags
Amber List (moderate evidence)	PEX26	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 7A (Zellweger) MIM#614872 Tags
Amber List (moderate evidence)	PEX3	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 10A (Zellweger) 614882 Tags
Amber List (moderate evidence)	PEX5	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Literature Phenotypes Peroxisome biogenesis disorder 2A (Zellweger) (MIM#214110) Tags
Amber List (moderate evidence)	PI4KA	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Amber Victorian Clinical Genetics Services Phenotypes Polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis, MIM# 616531 Tags
Amber List (moderate evidence)	SMO	1 review	Unknown	Sources Expert Review Amber Literature Phenotypes Curry-Jones syndrome, somatic mosaic MIM#601707 Tags somatic
Red List (low evidence)	CEP83	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Nephronophthisis 18, MIM# 615862 Tags
Red List (low evidence)	DAG1	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9 (MIM#616538) Tags
Red List (low evidence)	ENO1	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Literature Phenotypes Polymicrogyria, MONDO:0000087, ENO1-related Tags
Red List (low evidence)	EOMES	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Phenotypes Microcephaly, MONDO:0001149, EOMES-related Tags
Red List (low evidence)	INTS8	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Phenotypes Neurodevelopmental disorder with cerebellar hypoplasia and spasticity, MIM# 618572 Tags
Red List (low evidence)	MCF2	1 review 1 red	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Literature Phenotypes Perisylvian polymicrogyria Tags
Red List (low evidence)	PEX11B	2 reviews 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes ?Peroxisome biogenesis disorder 14B (MIM#614920) Tags
Red List (low evidence)	SHH	1 review 1 red	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Phenotypes Schizencephaly (MIM#269160) Tags disputed
Red List (low evidence)	SIX3	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Tags
Red List (low evidence)	SRD5A3	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Congenital disorder of glycosylation, type Iq (MIM#612379) Tags
Red List (low evidence)	SRPX2	1 review 1 red	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Phenotypes Rolandic epilepsy, mental retardation, and speech dyspraxia, MIM# 300643 Tags
Red List (low evidence)	TMEM216	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Phenotypes Joubert syndrome 2 (MIM#608091) Tags
Red List (low evidence)	TUBA8	1 review 1 red	BIALLELIC, autosomal or pseudoautosomal	Sources Australian Genomics Health Alliance Brain Malformations Flagship Expert Review Red Victorian Clinical Genetics Services Phenotypes Cortical dysplasia, complex, with other brain malformations 8, MIM# 613180 Tags

Polymicrogyria and Schizencephaly (Version 0.195)

16 reviewers

86 Entities

75 reviewed, 50 green

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

0 reviews

Sources

Tags

1 review

Sources

Phenotypes

Tags

2 reviews

Sources

Phenotypes

Tags

2 reviews

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

0 reviews

Sources

Tags

1 review

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

2 reviews

Sources

Phenotypes

Tags

2 reviews

Sources

Phenotypes

Tags

1 review

Sources

Phenotypes

Tags

2 reviews

Sources

Phenotypes

Tags

2 reviews

Sources