Abnormality of the skeletal system, and Type I diabetes mellitus

Diseases related with Abnormality of the skeletal system and Type I diabetes mellitus

In the following list you will find some of the most common rare diseases related to Abnormality of the skeletal system and Type I diabetes mellitus that can help you solving undiagnosed cases.


Top matches:

Low match DIABETES MELLITUS, INSULIN-DEPENDENT, 2


DIABETES MELLITUS, INSULIN-DEPENDENT, 2 Is also known as iddm2|insulin-dependent diabetes mellitus 2

Related symptoms:

  • Diabetes mellitus
  • Type I diabetes mellitus


SOURCES: MESH OMIM MENDELIAN

More info about DIABETES MELLITUS, INSULIN-DEPENDENT, 2

Low match DIABETES MELLITUS, INSULIN-DEPENDENT, 10; IDDM10


DIABETES MELLITUS, INSULIN-DEPENDENT, 10; IDDM10 Is also known as insulin-dependent diabetes mellitus 10

Related symptoms:

  • Diabetes mellitus
  • Type I diabetes mellitus


SOURCES: OMIM MESH MENDELIAN

More info about DIABETES MELLITUS, INSULIN-DEPENDENT, 10; IDDM10

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Other less relevant matches:

Low match DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1; NIDDM1


DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1; NIDDM1 Is also known as noninsulin-dependent diabetes mellitus 1

Related symptoms:

  • Diabetes mellitus
  • Type II diabetes mellitus
  • Type I diabetes mellitus


SOURCES: OMIM MESH MENDELIAN

More info about DIABETES MELLITUS, NONINSULIN-DEPENDENT, 1; NIDDM1

Low match DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM


DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM Is also known as noninsulin-dependent diabetes mellitus|maturity-onset diabetes|diabetes mellitus, type ii|t2d

Related symptoms:

  • Diabetes mellitus
  • Type II diabetes mellitus
  • Insulin resistance
  • Type I diabetes mellitus
  • Hyperinsulinemia


SOURCES: OMIM ORPHANET MENDELIAN

More info about DIABETES MELLITUS, NONINSULIN-DEPENDENT; NIDDM

Low match EPISODIC PAIN SYNDROME, FAMILIAL, 2; FEPS2


Familial episodic pain syndrome-2 is an autosomal dominant neurologic disorder characterized by adult-onset of paroxysmal pain mainly affecting the distal lower extremities (summary by Faber et al., 2012).For a discussion of genetic heterogeneity of familial episodic pain syndrome, see {615040}.

Related symptoms:

  • Pain
  • Diabetes mellitus
  • Type I diabetes mellitus
  • Hyperalgesia
  • Allodynia


SOURCES: ORPHANET OMIM MENDELIAN

More info about EPISODIC PAIN SYNDROME, FAMILIAL, 2; FEPS2

Low match PANCREATIC AGENESIS 2; PAGEN2


PANCREATIC AGENESIS 2; PAGEN2 Is also known as pancreatic hypoplasia, congenital 2

Related symptoms:

  • Global developmental delay
  • Diabetes mellitus
  • Small for gestational age
  • Hepatic failure
  • Type I diabetes mellitus


SOURCES: OMIM MENDELIAN

More info about PANCREATIC AGENESIS 2; PAGEN2

Low match PARTIAL PANCREATIC AGENESIS


Partial agenesis of the pancreas is characterized by the congenital absence of a critical mass of pancreatic tissue.

PARTIAL PANCREATIC AGENESIS Is also known as congenital pancreatic agenesis|pancreatic hypoplasia, congenital|pagen|partial agenesis of the pancreas

Related symptoms:

  • Growth delay
  • Failure to thrive
  • Intrauterine growth retardation
  • Diabetes mellitus
  • Malabsorption


SOURCES: ORPHANET OMIM MENDELIAN

More info about PARTIAL PANCREATIC AGENESIS

Low match PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE


PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE Is also known as papas|familial recurrent arthritis|papa syndrome|fra

Related symptoms:

  • Diabetes mellitus
  • Arthritis
  • Proteinuria
  • Type I diabetes mellitus
  • Acne


SOURCES: OMIM MENDELIAN

More info about PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE

Low match DIABETES MELLITUS, KETOSIS-PRONE; KPD


In addition to classic type 1 (see {222100}) and type 2 (see {125853}) diabetes mellitus, atypical presentations are seen, particularly in populations of African ancestry. Ketosis-prone diabetes, the most common atypical form, is characterized by an acute initial presentation with severe hyperglycemia and ketosis, as seen in classic type 1 diabetes, but after initiation of insulin therapy, prolonged remission is often possible with cessation of insulin therapy and maintenance of appropriate metabolic control. Metabolic studies show a markedly blunted insulin secretory response to glucose, partially reversible with the improvement of blood glucose control. Variable levels of insulin resistance are observed, especially in obese patients. Pancreatic beta-cell autoimmunity is a rare finding, and association with type 1 susceptibility HLA alleles is variable (Sobngwi et al., 2002).

Related symptoms:

  • Diabetes mellitus
  • Weight loss
  • Autoimmunity
  • Type II diabetes mellitus
  • Insulin resistance


SOURCES: ORPHANET OMIM MENDELIAN

More info about DIABETES MELLITUS, KETOSIS-PRONE; KPD

Top 5 symptoms//phenotypes associated to Abnormality of the skeletal system and Type I diabetes mellitus

Symptoms // Phenotype % cases
Diabetes mellitus Very Common - Between 80% and 100% cases
Type II diabetes mellitus Uncommon - Between 30% and 50% cases
Hyperglycemia Uncommon - Between 30% and 50% cases
Insulin resistance Rare - less than 30% cases
Glucose intolerance Rare - less than 30% cases
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Other less frequent symptoms

Patients with Abnormality of the skeletal system and Type I diabetes mellitus. may also develop some of the following symptoms:

Rare Symptoms - Less than 30% cases


Pancreatic hypoplasia Pyoderma gangrenosum Arthritis Proteinuria Acne Juvenile rheumatoid arthritis Pyoderma Autoimmunity Sterile arthritis Weight loss Maturity-onset diabetes of the young Polydipsia Polyuria Ketosis Ketoacidosis Diabetic ketoacidosis Neonatal insulin-dependent diabetes mellitus Malabsorption Maternal diabetes Global developmental delay Hyperinsulinemia Fasting hyperinsulinemia Decreased waist to hip ratio Pain Hyperalgesia Allodynia Small for gestational age Exocrine pancreatic insufficiency Hepatic failure Steatorrhea Growth delay Failure to thrive Intrauterine growth retardation Increased body weight Beta-cell dysfunction



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