Arthritis, and Depressivity

Diseases related with Arthritis and Depressivity

In the following list you will find some of the most common rare diseases related to Arthritis and Depressivity that can help you solving undiagnosed cases.


Top matches:

Medium match LEGG-CALVÉ-PERTHES DISEASE


Legg-Calve-Perthes disease (LCPD) is the term used to describe uni- or bilateral avascular necrosis (AVN) of the femoral head in children.

LEGG-CALVÉ-PERTHES DISEASE Is also known as legg-perthes disease|osteochondrosis of the capital femoral epiphysis|perthes disease|aseptic necrosis of the capital femoral epiphysis|lcp|osteochondritis of the capital femoral epiphysis

Related symptoms:

  • Short stature
  • Pain
  • Skeletal muscle atrophy
  • Abnormality of the dentition
  • Depressivity


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about LEGG-CALVÉ-PERTHES DISEASE

Medium match RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM


Related symptoms:

  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Ataxia
  • Anemia


SOURCES: OMIM MENDELIAN

More info about RETINITIS PIGMENTOSA AND ERYTHROCYTIC MICROCYTOSIS; RPEM

Medium match AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA


Autosomal dominant dopa-responsive dystonia (DYT5a) is a rare neurometabolic disorder characterized by childhood-onset dystonia that shows a dramatic and sustained response to low doses of levodopa (L-dopa) and that may be associated with parkinsonism at an older age.

AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA Is also known as hpd with marked diurnal fluctuation|gtpch1-deficient dopa-responsive dystonia|gtpch1-deficient drd|dyt5a|hereditary progressive dystonia with marked diurnal fluctuation|autosomal dominant segawa syndrome

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Scoliosis
  • Ataxia
  • Hypertension


SOURCES: ORPHANET MENDELIAN

More info about AUTOSOMAL DOMINANT DOPA-RESPONSIVE DYSTONIA

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Other less relevant matches:

Medium match DYSTONIA, DOPA-RESPONSIVE; DRD


DYSTONIA, DOPA-RESPONSIVE; DRD Is also known as dystonia, progressive, with diurnal variation|dystonia 5|segawa syndrome, autosomal dominant|dystonia, dopa-responsive, autosomal dominant|dopa-responsive dystonia, autosomal dominant|dystonia-parkinsonism with diurnal fluctuation|dyt5

Related symptoms:

  • Intellectual disability
  • Hearing impairment
  • Scoliosis
  • Nystagmus
  • Spasticity


SOURCES: ORPHANET OMIM MENDELIAN

More info about DYSTONIA, DOPA-RESPONSIVE; DRD

Medium match HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA


Hereditary hypophosphatemic rickets with hypercalciuria (HHRH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia and hypercalciuria associated with rickets and/or osteomalacia.

HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA Is also known as hypophosphatemia, x-linked|hpdr|hhrh|hyp|xlh|hypophosphatemic vitamin d-resistant rickets|vitamin d-resistant rickets, x-linked

Related symptoms:

  • Short stature
  • Hearing impairment
  • Growth delay
  • Neoplasm
  • Sensorineural hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about HEREDITARY HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA

Medium match JUVENILE HUNTINGTON DISEASE


Juvenile Huntington disease (JHD) is a form of Huntington disease (HD; see this term), characterized by onset of signs and symptoms before 20 years of age.

JUVENILE HUNTINGTON DISEASE Is also known as huntington chorea|jhd|juvenile huntington chorea

Related symptoms:

  • Seizures
  • Ataxia
  • Cognitive impairment
  • Anemia
  • Delayed speech and language development


SOURCES: OMIM ORPHANET MENDELIAN

More info about JUVENILE HUNTINGTON DISEASE

Medium match KNIEST DYSPLASIA


Kniest dysplasia is a severe type II collagenopathy characterized by a short trunk and limbs, prominent joints and midface hypoplasia (round face with a flat nasal root).

Related symptoms:

  • Short stature
  • Hearing impairment
  • Scoliosis
  • Micrognathia
  • Cleft palate


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about KNIEST DYSPLASIA

Medium match GIANT CELL ARTERITIS


Giant cell arteritis (GCA) is a large vessel vasculitis predominantly involving the arteries originating from the aortic arch and especially the extracranial branches of the carotid arteries.

GIANT CELL ARTERITIS Is also known as horton disease|giant cell arteritis|temporal arteritis|cranial arteritis|polymyalgia rheumatica|gca

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Muscle weakness
  • Ptosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about GIANT CELL ARTERITIS

Medium match ACROMEGALY


Acromegaly is an acquired disorder related to excessive production of growth hormone (GH) and characterized by progressive somatic disfigurement (mainly involving the face and extremities) and systemic manifestations.

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fatigue
  • Frontal bossing
  • Abnormality of the dentition


SOURCES: ORPHANET MENDELIAN

More info about ACROMEGALY

Medium match MARSHALL SYNDROME


Marshall syndrome is a malformation syndrome that is characterized by facial dysmorphism, severe hypoplasia of the nasal bones and frontal sinuses, ocular involvement, early-onset hearing loss, skeletal and anhidrotic ectodermal anomalies and short stature with spondyloepiphyseal dysplasia and early-onset osteoarthritis.

Related symptoms:

  • Short stature
  • Hearing impairment
  • Hypertelorism
  • Nystagmus
  • Micrognathia


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about MARSHALL SYNDROME

Top 5 symptoms//phenotypes associated to Arthritis and Depressivity

Symptoms // Phenotype % cases
Hearing impairment Common - Between 50% and 80% cases
Hypertension Uncommon - Between 30% and 50% cases
Arthralgia Uncommon - Between 30% and 50% cases
Osteoarthritis Uncommon - Between 30% and 50% cases
Short stature Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Arthritis and Depressivity. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Fatigue Rheumatoid arthritis Anxiety Ataxia Abnormality of the dentition Frontal bossing Bradykinesia Scoliosis Nystagmus Gait ataxia Rigidity Hyperhidrosis Myopia Abnormality of the skeletal system Gait disturbance Obsessive-compulsive behavior

Rare Symptoms - Less than 30% cases


Abnormal cerebellum morphology Tremor Irritability Hyperlordosis Involuntary movements Dystonia Motor delay Cerebral palsy Neoplasm Sensorineural hearing impairment Behavioral abnormality Paresis of extensor muscles of the big toe Abnormality of movement Muscle weakness Hyperreflexia Pain Spinal canal stenosis Conductive hearing impairment Thick lower lip vermilion Paresthesia Visual impairment Lens luxation Hypoplastic ilia Vitreoretinopathy Ectopia lentis Recurrent otitis media High myopia Retinal detachment Platyspondyly Joint stiffness Proptosis Diabetes mellitus Glaucoma Midface retrusion Malar flattening Short nose Kyphosis Depressed nasal bridge Ptosis Cataract Transient hyperphenylalaninemia Micrognathia Cough Weight loss Abnormality of the substantia nigra Cleft palate Decreased CSF homovanillic acid Hyperkinesis Optic disc pallor Fever Anemia Intellectual disability Talipes equinovarus Babinski sign Seizures Joint dislocation Progressive flexion contractures Pes cavus Hypothyroidism Sleep disturbance Parkinsonism Edema Abnormality of extrapyramidal motor function Focal dystonia Lower limb hyperreflexia Generalized dystonia Brisk reflexes Limb dystonia Postural tremor Impaired vibration sensation in the lower limbs Torticollis Horizontal nystagmus Impaired mastication Arteritis Glossitis Pericarditis Gangrene Gastrointestinal infarctions Abdominal aortic aneurysm Cerebral ischemia Amaurosis fugax Mediastinal lymphadenopathy Abnormality of the pleura Aortic dissection Abnormal thrombocyte morphology Arterial thrombosis Recurrent pharyngitis Double outlet right ventricle with subpulmonary ventricular septal defect without pulmonary stenosis Visual field defect Wide nose Mitral regurgitation Skeletal muscle atrophy Migraine Full cheeks Macroglossia Tapered finger Long face Retinal arteritis Synophrys Broad forehead Hypertrophic cardiomyopathy Coarse facial features Macrotia Mandibular prognathia Jaw claudication Elevated erythrocyte sedimentation rate Diplopia Diabetes insipidus Enlarged joints Visual loss Headache Renal insufficiency Blindness Optic atrophy Peripheral neuropathy Abnormal cartilage collagen Alopecia Flattened, squared-off epiphyses of tubular bones Splayed epiphyses Coronal cleft vertebrae Enlarged thorax Lumbar kyphoscoliosis Dumbbell-shaped long bone Arrhythmia Congenital hip dislocation Ophthalmoparesis Sudden cardiac death Vasculitis Meningitis Skin ulcer Rhegmatogenous retinal detachment Anorexia Epistaxis Hematuria Abdominal pain Hepatic failure Vertigo Thickened skin Delayed skeletal maturation Stroke Myalgia Aseptic necrosis Tall stature Large hands Hoarse voice Otitis media Sparse eyelashes Coxa valga Sparse and thin eyebrow Hypohidrosis Amblyopia Sparse scalp hair Cerebral calcification Esotropia Thickened calvaria Ectodermal dysplasia Bifid uvula Hypoplasia of the maxilla Flat face Genu valgum Congenital cataract Hypotrichosis Sparse eyebrow Aplasia cutis congenita Brachycephaly Abnormal vitreous humor morphology Meningeal calcification Small proximal tibial epiphyses Wide tufts of distal phalanges Irregular distal femoral epiphysis Irregular proximal tibial epiphyses Macrodontia of permanent maxillary central incisor Calcification of falx cerebri Hypoplastic frontal sinuses Pierre-Robin sequence Absent frontal sinuses Ulnar bowing Anhidrotic ectodermal dysplasia Concave nasal ridge Thick upper lip vermilion Hypoplasia of the zygomatic bone Radial bowing Sparse hair Long philtrum Generalized hirsutism Generalized hyperpigmentation Dysuria Abnormality of the endocrine system Abnormal toenail morphology Broad foot Growth hormone excess Joint swelling Palpebral edema Impotence Deep palmar crease Hypoplastic pelvis Acne Growth abnormality Sleep apnea Widely spaced teeth Acanthosis nigricans Abnormality of the fingernails Neoplasm of the endocrine system Anterior hypopituitarism Anteverted nares Abnormality of reproductive system physiology Wide nasal bridge Epicanthus High palate Low-set ears Strabismus Hypertelorism Cortical diaphyseal thickening of the upper limbs Broad jaw Pheochromocytoma Macrodactyly Dysmenorrhea Pituitary prolactin cell adenoma Deep plantar creases Galactorrhea Hypersomnia Paraganglioma Long penis Disproportionate short-trunk short stature Spondyloepiphyseal dysplasia Tracheal stenosis Hyperphosphatemia Fibular bowing Hypocalciuria Renal phosphate wasting Hypophosphatemic rickets Tetany Elevated circulating parathyroid hormone level Renal tubular dysfunction Polyostotic fibrous dysplasia Spinal cord compression Ankylosis Decreased serum iron Osteomalacia Glycosuria Hyperparathyroidism Tibial bowing Hypomineralization of enamel Pseudo-fractures Hypophosphatemia Cerebellar atrophy Mental deterioration Aggressive behavior Decreased mean corpuscular volume Hyperactivity Epiretinal membrane Myoclonus Dementia Ventriculomegaly Trapezoidal distal femoral condyles Dysphagia Dysarthria Delayed speech and language development Cognitive impairment Tertiary hyperparathyroidism Shortening of the talar neck Flattening of the talar dome Femoral bowing Bowing of the legs Abnormality of the cerebral white matter Dysphonia Torsion dystonia Upper motor neuron dysfunction Hyperactive deep tendon reflexes Resting tremor Gaze-evoked nystagmus Spastic diplegia Confusion Oromandibular dystonia Paraplegia Spastic paraplegia Abnormal pyramidal sign Difficulty walking Encephalopathy Hypertonia Spasticity Parkinsonism with favorable response to dopaminergic medication Writer's cramp Metaphyseal irregularity Bone pain Rickets Hypercalcemia Elevated alkaline phosphatase Hypercalciuria Abnormality of pelvic girdle bone morphology Nephrocalcinosis Hypocalcemia Left ventricular hypertrophy Axial dystonia Ventricular hypertrophy Ring scotoma Photoreceptor layer loss on macular OCT Growth delay Fixed facial expression Obsessive-compulsive trait Infantile encephalopathy Elliptocytosis Abnormality of eye movement Delayed epiphyseal ossification Severe short stature Hip dislocation Retinopathy Umbilical hernia Skeletal dysplasia Retrognathia Pallor Inguinal hernia Micromelia Nyctalopia Abnormality of skin pigmentation Retinal atrophy Respiratory distress Short neck Macrocephaly Anisocytosis Global developmental delay Round face Macular edema Short thorax Lower limb asymmetry Bell-shaped thorax Glossoptosis Tracheomalacia Hip contracture Arthropathy Chorioretinal atrophy Flared metaphysis Cartilage destruction Neonatal respiratory distress Avascular necrosis of the capital femoral epiphysis Coxa vara Rhizomelia Abnormality of epiphysis morphology Abnormality of the metaphysis Synovitis Flexion contracture Juvenile rheumatoid arthritis Infertility Type II diabetes mellitus Slurred speech Incoordination Schizophrenia Clumsiness Broad-based gait Progressive neurologic deterioration Generalized-onset seizure Akinesia Neuronal loss in central nervous system Brain atrophy Chorea Gliosis Progressive cerebellar ataxia Neurodegeneration Falls Personality changes Hypokinesia Poikilocytosis Paranoia Retinal pigment epithelial atrophy Oral motor hypotonia Frequent temper tantrums Suicidal ideation Neuronal loss in basal ganglia Abnormal involuntary eye movements Mania Testicular atrophy Muscle fibrillation Dilated fourth ventricle Chronic bronchitis Head tremor Upper limb undergrowth Restlessness Cerebellar vermis atrophy Bronchitis Small distal femoral epiphysis



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