| Diseases |
Alias |
|
| Cerebrooculofacioskeletal Syndrome 2 |
|
COFS2
|
Cerebro-Oculo-Facio-Skeletal Syndrome 2
|
|
Cofs Syndrome
|
|
|
| Xeroderma Pigmentosum, Complementation Group D |
|
Xeroderma Pigmentosum, Group D
|
Xpdc
|
|
Xeroderma Pigmentosum Iv
|
XPD
|
|
Xeroderma Pigmentosum Group D
|
Xeroderma Pigmentosum Viii
|
|
Xp Group D
|
Xp Group H
|
|
Xp4
|
Xp8
|
|
Xph
|
Xp, Group D
|
|
Xp4 Xeroderma Pigmentosum Viii, Formerly
|
Xp8, Formerly
|
|
Xp, Group H, Formerly
|
Xph, Formerly
|
|
Xeroderma Pigmentosum Complementation Group D
|
XP-D
|
|
Xp-D/Cs
|
|
|
| Trichothiodystrophy 1, Photosensitive |
|
TTD1
|
Tay Syndrome
|
|
Trichothiodystrophy With Congenital Ichthyosis
|
Photosensitive Trichothiodystrophy
|
|
Ibids Syndrome
|
Ttdp
|
|
Ichthyosiform Erythroderma With Hair Abnormality And Mental And Growth Retardation
|
Ichthyosis, Congenital, With Trichothiodystrophy
|
|
Pibids Syndrome
|
Photosensitive Trichothiodystrophy 1
|
|
Trichothiodystrophy, Photosensitive
|
Sulfur-Deficient Brittle Hair Syndrome
|
|
Ttd-P
|
Ichthyosis With Brittle Hair, Intellectual Impairment, Decreased Fertility And Short Stature
|
|
Trichothiodystrophy Photosensitive
|
Trichothiodystrophy, Type 1
|
|
Tricho-Thiodystrophy Disorder
|
Trichothiodystrophy Syndromes
|
|
Amish Brittle Hair Brain Syndrome
|
|
|
| Trichothiodystrophy |
|
Ttd
|
Amish Brittle Hair Syndrome
|
|
Bids Syndrome
|
Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome
|
|
Ibids
|
Pibids
|
|
Trichothiodystrophy Syndromes
|
|
|
| Xeroderma Pigmentosum, Variant Type |
|
Xeroderma Pigmentosum
|
XPV
|
|
Xeroderma Pigmentosum Variant Type
|
Xeroderma Pigmentosum With Normal Dna Repair Rates
|
|
Photosensitivity With Defective Dna Synthesis
|
Xp
|
|
De Sanctis-Cacchione Syndrome
|
Desanctis-Cacchione Syndrome
|
|
Xeroderma Pigmentosa
|
Xerodermic Idiocy
|
|
Xeroderma Pigmentosum Variant
|
Xp - [Xeroderma Pigmentosum]
|
|
Atrophoderma Pigmentosum
|
|
|
| Trichothiodystrophy 3, Photosensitive |
|
TTD3
|
Trichothiodystrophy, Complementation Group A
|
|
Ttda
|
Photosensitive Trichothiodystrophy 3
|
|
Trichothiodystrophy Complementation Group A
|
|
|
| Xeroderma Pigmentosum-Cockayne Syndrome Complex |
|
|
| Hypotrichosis Simplex |
|
Hereditary Hypotrichosis Simplex
|
Hhs
|
|
|
| Cerebrooculofacioskeletal Syndrome 1 |
|
Cofs Syndrome
|
COFS1
|
|
Pena-Shokeir Syndrome Type 2
|
Cofs
|
|
Pena-Shokeir Syndrome, Type Ii
|
Cerebrooculofacioskeletal Syndrome
|
|
Cerebro-Oculo-Facio-Skeletal Syndrome 1
|
Pena Shokeir Syndrome Type 2
|
|
|
| Corpus Callosum, Agenesis Of |
|
Corpus Callosum Agenesis
|
Agenesis Of The Corpus Callosum
|
|
Isolated Corpus Callosum Agenesis
|
Acc
|
|
Non Rare In Europe: Isolated Corpus Callosum Agenesis
|
Congenital Malformation Of Corpus Callosum
|
|
Deformity Of Corpus Callosum
|
Absence Of Corpus Callosum
|
|
Absent Corpus Callosum
|
Acc - [Agenesis Of Corpus Callosum]
|
|
Aplasia Of Corpus Callosum
|
Congenital Absence Of Corpus Callosum
|
|
Hypoplastic Corpus Callosum
|
Hypoplasia Of Corpus Callosum
|
|
|
| Intellectual Disability - Hypoplastic Corpus Callosum - Preauricular Tag |
|
Da Silva Syndrome
|
Intellectual Disability-Hypoplastic Corpus Callosum-Preauricular Tag Syndrome
|
|
|
| Cockayne Syndrome |
|
Cockayne'S Syndrome
|
Dwarfism-Retinal Atrophy-Deafness Syndrome
|
|
Neill-Dingwall Syndrome
|
Progeria-Like Syndrome
|
|
Progeroid Nanism
|
Cs
|
|
|
| Craniopharyngioma |
|
Neoplasm Of Rathke'S Pouch
|
Adamantinomatous Tumor
|
|
Craniopharyngeal Duct Tumor
|
Dysodontogenic Epithelial Tumor
|
|
Rathke'S Pouch Tumor
|
|
|
| Metachromatic Leukodystrophy |
|
Arylsulfatase A Deficiency
|
MLD
|
|
Arsa Deficiency
|
Sulfatide Lipidosis
|
|
Metachromatic Leukoencephalopathy
|
Cerebral Sclerosis, Diffuse, Metachromatic Form
|
|
Cerebroside Sulfatase Deficiency
|
Leukodystrophy, Metachromatic
|
|
Pseudoarylsulfatase A Deficiency
|
Leukodystrophy Metachromatic
|
|
Sulfatidosis
|
Metachromatic Leukodystrophy, Late Infantile
|
|
Metachromatic Leukodystrophy Variant
|
Deficiency Of Cerebroside-Sulfatase
|
|
Scholz Cerebral Sclerosis
|
Sulfatide Lipoidosis
|
|
Cerebral Sclerosis Diffuse Metachromatic Form
|
Arylsulfatase A Deficiency Disease
|
|
Cerebroside Sulphatase Deficiency Disease
|
Greenfield Disease
|
|
Metachromatic Leukodystrophy, Adult
|
Metachromatic Leukodystrophy, Juvenile
|
|
Leukodystrophy Metachromatic Adult
|
Leukodystrophy Metachromatic Juvenile
|
|
Leukodystrophy Metachromatic Late Infantile
|
Metachromatic Leukodystrophy, Adult Type
|
|
Metachromatic Leukodystrophy, Juvenile Type
|
Metachromatic Leukodystrophy, Infant
|
|
Greenfield'S Disease
|
|
|
| Skin Carcinoma |
|
Skin Cancer
|
Carcinoma Of Skin
|
|
Ca - Skin Cancer
|
Cancer Of Skin
|
|
Malignant Neoplasm Of Skin
|
Melanoma And Non-Melanoma Skin Cancer
|
|
Skin Cancers
|
Cancer, Skin
|
|
|
| Hepatoblastoma |
|
|
| Parkinsonism With Spasticity, X-Linked |
|
X-Linked Parkinsonism-Spasticity Syndrome
|
XPDS
|
|
X-Linked Parkinsonism With Spasticity
|
|
|
| Cerebrooculofacioskeletal Syndrome |
|
Cerebro-Oculo-Facio-Skeletal Syndrome
|
Cofs Syndrome
|
|
Pena-Shokeir Syndrome Type 2
|
Pena Shokeir Syndrome Type 2
|
|
|
| Basal Cell Carcinoma |
|
Basal Cell Cancer
|
Basal Cell Neoplasm
|
|
Basal Cell Carcinoma Of Skin
|
Malignant Basal Cell Tumor
|
|
Basal Cell Tumor
|
Epithelioma Basal Cell
|
|
Malignant Basal Cell Neoplasm
|
Rodent Ulcer
|
|
Carcinoma Basal Cell
|
Neoplasms, Basal Cell
|
|
Basal Cell Carcinomas
|
Experimental Organism Basal Cell Carcinoma
|
|
Nodulo-Ulcerative Basal Cell Carcinoma
|
Basalioma
|
|
Basal Cell Epithelioma Of Skin
|
Bcc - [Basal Cell Carcinoma] Of Skin
|
|
Rodent Ulcer Of Skin
|
Rodent Ulcer Of Unspecified Site
|
|
Basal Cell Epithelioma Of Unspecified Site
|
|
|
| Xeroderma Pigmentosum, Complementation Group G |
|
Xeroderma Pigmentosum, Group G
|
Xeroderma Pigmentosum Vii
|
|
Xp7
|
XPG
|
|
Xeroderma Pigmentosum Group G
|
Xp Group G
|
|
Xp, Group G
|
Xpgc
|
|
Xeroderma Pigmentosum, Group G/Cockayne Syndrome
|
Xeroderma Pigmentosum, Type 7
|
|
Xeroderma Pigmentosum Complementation Group G
|
XP-G
|
|
Xp-G/Cs
|
Xeroderma Pigmentosum Group G/Cockayne Syndrome
|
|
|
| Ichthyosis |
|
Ichthyoses
|
Non-Syndromic Ichthyosis
|
|
Congenital Ichthyosis
|
|
|
| Xeroderma Pigmentosum, Complementation Group B |
|
Xeroderma Pigmentosum Group B
|
Xeroderma Pigmentosum, Group B
|
|
XPB
|
Xpbc
|
|
Xp Group B
|
Xp, Group B
|
|
Xeroderma Pigmentosum Complementation Group B
|
XP-B
|
|
Xeroderma Pigmentosum Group B With Cockayne Syndrome
|
Xeroderma Pigmentosum Ii
|
|
Xp2
|
Xp-B/Cs
|
|
|
| Testicular Cancer |
|
Testis Cancer
|
Testicular Carcinoma
|
|
Testicular Neoplasms
|
Malignant Neoplasm Of Testis
|
|
Childhood Neoplasm Of The Testis
|
Neoplasm Of Testis
|
|
Pediatric Testicular Neoplasm
|
Testicular Tumor
|
|
Testis Neoplasm
|
Testicular Tumors
|
|
Testicular Neoplasm
|
Testicular Malignant Germ Cell Tumor
|
|
Childhood Testicular Neoplasm
|
Carcinoma Of The Testis
|
|
Cancer Of Testis
|
Malignant Neoplasm Of Testis, Nos
|
|
Malignant Neoplasm Of Testis, Unspecified
|
Malignant Tumour Of Testis
|
|
Testicle Cancer
|
Primary Malignant Neoplasm Of Testis
|
|
|
| Xeroderma Pigmentosum, Complementation Group F |
|
Xeroderma Pigmentosum, Group F
|
Xeroderma Pigmentosum Vi
|
|
Xp6
|
Xeroderma Pigmentosum, Type F/Cockayne Syndrome
|
|
XPF
|
Xp, Group F
|
|
Xeroderma Pigmentosum Group F
|
Xp Group F
|
|
Xeroderma Pigmentosum, Type 6
|
Xeroderma Pigmentosum Complementation Group F
|
|
XP-F
|
Xeroderma Pigmentosum Type F/Cockayne Syndrome
|
|
XPF/CS
|
|
|
| Xeroderma Pigmentosum, Complementation Group A |
|
Xeroderma Pigmentosum Group A
|
Xp1
|
|
Xeroderma Pigmentosum, Group A
|
XPA
|
|
Xeroderma Pigmentosum I
|
Xeroderma Pigmentosum Complementation Group A
|
|
Xp Group A
|
Xp, Group A
|
|
Xeroderma Pigmentosum 1
|
Xeroderma Pigmentosum, Type 1
|
|
XP-A
|
|
|
| Fanconi Anemia, Complementation Group A |
|
Fanconi Anemia
|
Fanconi Pancytopenia
|
|
Fanconi Anemia Complementation Group A
|
FANCA
|
|
Fa
|
Fanconi Panmyelopathy
|
|
Fanconi'S Anemia
|
Fanconi Anaemia
|
|
Fanconi'S Anaemia
|
Fanconi Hypoplastic Anemia
|
|
Estren-Dameshek Variant Of Fanconi Anemia
|
Estren-Dameshek Variant Of Fanconi Pancytopenia
|
|
Fanconi Anemia Estren-Dameshek Variant
|
Fanconis Anemia
|
|
|
| Uv-Sensitive Syndrome |
|
Uvss
|
Uv Sensitive Syndrome
|
|
Ultraviolet Sensitive Syndrome
|
|
|
| Trichothiodystrophy 2, Photosensitive |
|
TTD2
|
Photosensitive Trichothiodystrophy 2
|
|
|
| De Sanctis-Cacchione Syndrome |
|
Xerodermic Idiocy
|
Xeroderma Pigmentosum With Neurologic Manifestation
|
|
DSC
|
Xerodermic Idiocy Of De Sanctis And Cacchione
|
|
|
| Mucositis |
|
Inflammatory Disease Of Mucous Membrane
|
Gastrointestinal Mucositis
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Susceptibility To
|
Lung Cancer, Protection Against
|
|
Adenocarcinoma Of Lung, Somatic
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
|
Nonsmall Cell Lung Cancer
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Neutropenia |
|
|
| Warsaw Breakage Syndrome |
|
|
| Bladder Cancer |
|
Urinary Bladder Cancer
|
Bladder Carcinoma
|
|
Urinary Bladder Carcinoma
|
Bladder Neoplasm
|
|
Bladder Tumor
|
Cancer, Bladder
|
|
Malignant Neoplasm Of Urinary Bladder
|
Carcinoma Of Bladder
|
|
Bladder Cancer, Somatic
|
Tumor Of The Bladder
|
|
Carcinoma Of Urinary Bladder
|
Bladder Carcinoma Urinary
|
|
Cancer Of The Urinary Bladder
|
Cancer, Urinary Bladder
|
|
Malignant Bladder Neoplasm
|
Malignant Bladder Tumor
|
|
Neoplasm Of The Bladder
|
Neoplasm Of The Urinary Bladder
|
|
Tumor Of The Urinary Bladder
|
Urinary Bladder Neoplasm
|
|
BLC
|
Urothelial Carcinoma Of The Bladder
|
|
Bladder Tumors
|
Urinary Bladder Neoplasms
|
|
Bladder Cancer Nos
|
Vesical Cancer Nos
|
|
Malignant Neoplasm Of Bladder, Part Unspecified
|
Malignant Tumour Of Urinary Bladder
|
|
Primary Malignant Neoplasm Of Bladder
|
|
|
| Xeroderma Pigmentosum, Complementation Group C |
|
Xeroderma Pigmentosum, Group C
|
XPC
|
|
Xpcc
|
Xeroderma Pigmentosum Iii
|
|
Xp3
|
Xeroderma Pigmentosum Group C
|
|
Xp Group C
|
Xp, Group C
|
|
Xeroderma Pigmentosum, Type 3
|
Xeroderma Pigmentosum Complementation Group C
|
|
XP-C
|
|
|
| Neuroma |
|
|
| Ocular Cancer |
|
Eye Neoplasm
|
Eye Carcinoma
|
|
Eye Cancer
|
Eye Neoplasms
|
|
Malignant Eye Neoplasm
|
Neoplasm Of Eye
|
|
Neoplasm Of Eye Proper
|
Ocular Tumor
|
|
Carcinoma Of Eye
|
Ocular Carcinoma
|
|
Malignant Tumor Of Eye
|
|
|
| Xfe Progeroid Syndrome |
|
Xpf-Ercc1 Progeroid Syndrome
|
XFEPS
|
|
|
| Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant |
|
Kid Syndrome
|
Keratitis-Ichthyosis-Deafness Syndrome
|
|
Senter Syndrome
|
KIDAD
|
|
Kid Syndrome, Autosomal Dominant
|
Autosomal Dominant Keratitis-Ichthyosis-Deafness Syndrome
|
|
Ichthyosis Hystrix Rheydt Type
|
Kid/Hid Syndrome
|
|
Keratitis-Ichthyosis-Deafness/Hystrix-Like Ichthyosis-Deafness Syndrome
|
Keratitis Ichthyosis And Deafness Syndrome
|
|
Autosomal Dominant Kid Syndrome
|
Keratitis, Ichthyosis, And Deafness Syndrome
|
|
Ichthyosiform Erythroderma, Corneal Involvement, And Deafness
|
Keratitis, Ichthyosis, And Deafness
|
|
Keratitis-Ichthyosis-Hearing Loss/Hystrix-Like Ichthyosis-Hearing Loss Syndrome
|
|
|
| Cockayne Syndrome A |
|
Cockayne Syndrome Type 1
|
Cockayne Syndrome, Type A
|
|
Cockayne Syndrome Type I
|
CSA
|
|
Cockayne Syndrome Classic Form
|
Cockayne Syndrome Classical
|
|
Cockayne Syndrome Type A
|
Ckn1
|
|
|
| Cockayne Syndrome B |
|
Cockayne Syndrome Type 2
|
Cockayne Syndrome, Type B
|
|
Cockayne Syndrome Type Ii
|
CSB
|
|
Cockayne Syndrome 2
|
Cockayne Syndrome Type B
|
|
Ckn2
|
Cockayne Syndrome, Type Ii
|
|
|
| Skin Benign Neoplasm |
|
Neoplasm Of Skin By Site
|
Tumor Of The Skin
|
|
Skin Tumor
|
Benign Neoplasm Of Skin
|
|
Skin Neoplasms
|
|
|
| Rothmund-Thomson Syndrome, Type 2 |
|
Rothmund-Thomson Syndrome
|
Rts
|
|
RTS2
|
Poikiloderma Of Rothmund-Thomson
|
|
Rothmund-Thomson Syndrome Type 2
|
Congenital Poikiloderma
|
|
Poikiloderma Congenitale
|
Poikiloderma Atrophicans And Cataract
|
|
Poikiloderma Congenitale Of Rothmund-Thomson
|
Poikiloderma Of Rothmund-Thomson Type 2
|
|
Rothmund-Thomson Syndrome 2
|
Erythrokeratodermia Variabilis
|
|
|
| Cataract |
|
Cataracts
|
Cat - [Cataract]
|
|
Cataract Form
|
Lens Opacity
|
|
Lens Opacities
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
|
Ovarian Neoplasms
|
Ovarian Cancers
|
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Parkinson Disease 2, Autosomal Recessive Juvenile |
|
Young-Onset Parkinson Disease
|
PARK2
|
|
Pdj
|
Autosomal Recessive Juvenile Parkinson Disease 2
|
|
Epdf
|
Parkinson Disease, Juvenile, Type 2
|
|
Parkinson'S Disease 2
|
Autosomal Recessive Juvenile Parkinson Disease
|
|
Early-Onset Parkinson Disease
|
Parkinson Disease 2
|
|
Parkinson Disease, Juvenile, Autosomal Recessive
|
Parkinsonism, Early-Onset, With Diurnal Fluctuation
|
|
Autosomal Recessive Juvenile Parkinson'S Disease 2
|
Jp
|
|
Juvenile Parkinsonism
|
Parkinson Disease Autosomal Recessive, Early Onset
|
|
Parkinsonism, Early Onset, With Diurnal Fluctuation
|
Yopd
|
|
Autosomal Recessive Early-Onset Parkinson Disease Type 2
|
Chromosome 6-Linked Autosomal Recessive Parkinsonism
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Early-Onset Parkinsonism With Diurnal Fluctuation
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Parkinsonism Young Adult Onset
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Parkinson Disease, Type 2
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Parkinsonism, Juvenile
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| Microcephaly |
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Microencephaly
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Microcephalus
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Microcephalic
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Nanocephaly
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Congenital Microcephaly
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Brain Hypoplasia
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Brain Nondevelopment
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Cephalic Hypoplasia
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Undeveloped Cerebrum
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Undeveloped Brain
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Micrencephalon
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Micrencephaly
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| Prostate Cancer |
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Prostate Carcinoma
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Prostate Cancer, Familial
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Prostate Neoplasm
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Prostate Cancer, Somatic
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Prostate Cancer, Susceptibility To
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Prostatic Cancer
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Prostatic Neoplasms
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Hereditary Prostate Cancer
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Prostatic Neoplasm
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Cancer Of Prostate
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Carcinoma Of Prostate
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Familial Prostate Cancer
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Familial Prostate Carcinoma
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Malignant Tumor Of Prostate
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Malignant Neoplasm Of Prostate
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Prostate Cancer, Familial, Susceptibility To
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Malignant Tumor Of The Prostate
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Ngp - New Growth Of Prostate
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Tumor Of The Prostate
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Prostate Cancer, Hereditary
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Cancer Of The Prostate
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Malignant Neoplasm Of The Prostate
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Prostatic Carcinoma
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PC
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Prca
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Cancer, Prostate
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Malignant Prostatic Tumour
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Malignant Tumour Of Prostate
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Primary Prostate Cancer
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Primary Malignant Neoplasm Of Prostate
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Prostate Gland Cancer
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| Aplastic Anemia |
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Aplastic Anemia, Susceptibility To
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Anemia Aplastic
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Idiopathic Aplastic Anemia
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Secondary Aplastic Anemia
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Idiopathic Bone Marrow Failure
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Aplastic Anemia Idiopathic
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AA
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Anemia, Aplastic
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Aplastic Anemia, Idiopathic
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Erythroid Aplasia
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Aa - [Aplastic Anaemia]
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Haematopoietic Aplasia
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Aleukia Haemorrhagica
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Anaemia Due To Decreased Red Cell Production
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Aplasia Bone Marrow
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Aplastic Bone Marrow
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Hypoplastic Anaemia Nos
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Myeloid Bone Marrow Aplasia
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Pancytopenia
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Panhaematopenia
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Hypoproliferative Anaemia
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Medullary Hypoplasia
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Red Blood Cells Hypoplastic Anaemia
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Panmyelophthisis
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Panhemocytopenia
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Refractive Hypoproliferative Anaemia
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Toxic Anaemia
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Toxic Aplastic Anaemia
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Aplastic Anaemia Due To Toxic Cause
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Idiopathic Aplastic Anaemia Nos
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| Lynch Syndrome |
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Hereditary Nonpolyposis Colon Cancer
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Hereditary Nonpolyposis Colorectal Cancer
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Hereditary Nonpolyposis Colorectal Carcinoma
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Hereditary Nonpolyposis Colorectal Neoplasms
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Familial Nonpolyposis Colon Cancer
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Hnpcc
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Coca 1
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Hereditary Defective Mismatch Repair Syndrome
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Hereditary Non-Polyposis Colon Cancer
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Hereditary Non-Polyposis Colon Cancer Syndrome
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Hereditary Non-Polyposis Colorectal Cancer
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Hereditary Non-Polyposis Colorectal Cancer Syndrome
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Hereditary Nonpolyposis Colon Cancer Syndrome
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Hereditary Nonpolyposis Colorectal Cancer Syndrome
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Hereditary Nonpolyposis Colorectal Neoplasm
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Hnpcc - Hereditary Nonpolyposis Colon Cancer
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Cancer Family Syndrome
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Familial Nonpolyposis Colorectal Cancer
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Colon Cancer, Familial Nonpolyposis
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Colorectal Neoplasms, Hereditary Nonpolyposis
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Cancer, Colorectal, Nonpolyposis, Hereditary
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Colorectal Cancer, Hereditary Nonpolyposis, Type 1
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| Melanoma, Cutaneous Malignant 1 |
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Familial Melanoma
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Melanoma, Cutaneous Malignant, Susceptibility To, 1
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Melanoma, Malignant
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CMM1
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Melanoma, Cutaneous Malignant
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Cmm
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Familial Atypical Mole-Malignant Melanoma Syndrome
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Fammm
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Melanoma, Familial
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Mlm
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Dysplastic Nevus Syndrome, Hereditary
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Dns
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B-K Mole Syndrome
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Melanoma, Cutaneous Malignant, 1
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Malignant Melanoma, Cutaneous
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Melanoma, Cutaneous, Malignant, Susceptibility To, Type 1
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Dysplastic Nevus Syndrome
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Cutaneous Melanoma
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Familial Atypical Mole Melanoma Syndrome
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Hereditary Melanoma
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| Hereditary Breast Ovarian Cancer Syndrome |
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Hereditary Breast And Ovarian Cancer Syndrome
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Brca1- And Brca2-Associated Hereditary Breast And Ovarian Cancer
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Breast And/Or Ovarian Cancer
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Breast And Ovarian Cancer Syndrome
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Hboc Syndrome
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Hereditary Breast And Ovarian Cancer
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Brca1- Brca2-Associated Hboc
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| Congenital Nervous System Abnormality |
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Congenital Neurologic Anomaly
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Congenital Nervous System Disorder
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